Antibacterial agents

ABSTRACT

Antibacterial compounds of formula I are provided: 
     
       
         
         
             
             
         
       
     
     As well as stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof; pharmaceutical compositions comprising such compounds; methods of treating bacterial infections by the administration of such compounds; and processes for the preparation of the compounds.

This application is a continuation of U.S. patent application Ser. No. 10/754,928, now abandoned, filed Jan. 8, 2004, which claims benefit of priority to the following U.S. Provisional Patent Applications: U.S. Ser. No. 60/438,523, filed Jan. 8, 2003; U.S. Ser. No. 60/466,974, filed Apr. 30, 2003; and U.S. Ser. No. 60/520,211 filed Nov. 13, 2003; each of which is incorporated herein by reference in its entirety for any purpose.

FIELD OF THE INVENTION

This invention pertains generally to treating infections caused by gram-negative bacteria. More specifically, the invention described herein pertains to treating gram-negative infections by inhibiting activity of UDP-3-O—(R-3-hydroxydecanoyl)-N-acetylglucosamine deacetylase (LpxC). The present invention provides small molecule inhibitors of LpxC, pharmaceutical formulations containing such inhibitors, methods of treating patients with such pharmaceutical formulations, and to methods of preparing such pharmaceutical formulations and inhibitors. The inhibitors can be used to treat Gram-negative infections of patients alone and in combination with other antibacterials.

BACKGROUND OF THE INVENTION

Over the past several decades, the frequency of antimicrobial resistance and its association with serious infectious diseases have increased at alarming rates. The increasing prevalence of resistance among nosocomial pathogens is particularly disconcerting. Of the over 2 million nosocomial infections occurring each year in the United States, 50 to 60% are caused by antimicrobial-resistant strains of bacteria. This high rate of resistance increases the morbidity, mortality, and costs associated with nosocomial infections. In the United States, nosocomial infections are thought to contribute to or cause more than 77,000 deaths per year and cost approximately $5 to $10 billion annually. Among Gram-positive organisms, the most important resistant pathogens are methicillin-(oxacillin-) resistant Staphylococcus aureus, β-lactam-resistant and multidrug-resistant pneumococci, and vancomycin-resistant enterococei. Important causes of Gram-negative resistance include extended-spectrum β-lactamases (ESBLs) in Klebsiella pneumoniae, Escherichia coli, and Proteus mirabilis, high-level third-generation cephalosporin (Amp C) β-lactamase resistance among Enterobacter species and Citrobacter freundii, and multidrug-resistance genes observed in Pseudomonas aeruginosa, Acinetobacter, and Stenotrophomonas maltophilia. (Jones R N 2001 Chest 119 (supplement), 397S-404S: Resistance patterns among nosocomial pathogens: Trends over the past few years.)

The problem of antibacterial resistance is compounded by the existence of bacterial strains resistant to multiple antibacterials. For example, Pseudomonas aeruginosa isolates resistant to fluoroquinolones are virtually all resistant to additional antibacterials (Sahm D F et al 2001 Antimicrobial Agents and Chemotherapy 45, 267-274: Evaluation of current activities of fluoroquinolones against gram-negative bacilli using centralized in vitro testing and electronic surveillance.)

Thus there is a need for new antibacterials, particularly antibacterials with novel mechanisms of action. Most of the antibacterial discovery effort in the pharmaceutical industry is aimed at development of drugs effective against gram-positive bacteria. However, there is also a need for new gram-negative antibacterials. Gram-negative bacteria are in general more resistant to a large number of antibacterials and chemotherapeutic agents than are gram-positive bacteria. A survey of recently reported antibacterials of natural origin showed that over 90% lacked activity against Escherichia coli, although they were active against gram-positive bacteria. The outer membrane of gram-negative bacteria contributes to this intrinsic resistance by acting as an efficient permeability barrier, because the narrow porin channels limit the penetration of hydrophilic solutes and the low fluidity of the lipopolysaccharide leaflet slows down the inward diffusion of lipophilic solutes. A second mechanism contributes to the intrinsic resistance of gram-negative bacteria. Recent studies showed that multiple drug efflux pumps, sometimes with unusually broad specificity, act as this second factor to create the general intrinsic resistance of gram-negative bacteria. When their expression levels are elevated as a consequence of physiological regulation or genetic alteration, they can frequently produce impressive levels of resistance to a wide variety of antimicrobial agents. (Nikaido H 1998 Clinical Infectious Diseases 27(Suppl 1), S32-41: Antibacterial resistance caused by gram-negative multidrug efflux pumps.)

Historically, most development of antimicrobial agents has been relatively empirical. Active compounds have generally been found via screening soil, sewage, water, and other natural substances to detect antimicrobial-producing organisms, or by screening various chemical compounds. Once a leading candidate has been found and its chemical structure determined, a series of analogs is made to identify an optimal compound for further clinical development. A more rational approach involves the defining of new targets, such as genes or enzymatic functions, responsible for a crucial cellular essential activity. Once this has been done, inhibitors or blockers of the function or gene product can be developed.

In order to identify potential targets for novel gram-negative antibacterial agents, studies aimed at identifying all essential and important genes in Pseudomonas aeruginosa have been performed. Among the essential genes identified was lpxC, that encodes the enzyme uridyldiphospho-3-O—(R-hydroxydecanoyl)-N-acetylglucosamine deacetylase (LpxC). This enzyme is the first committed step in the synthesis of lipid A, the lipid moiety of lipopolysaccharide, that is an essential component of all gram-negative bacteria. It therefore is an attractive target for novel antibacterials. In order to be useful as antibacterial agents, LpxC inhibitors would not only have to inhibit the enzymatic activity of LpxC from a variety of bacteria, but would have to defeat the intrinsic resistance mechanisms of gram-negative bacteria, as described above: they would have to penetrate the outer membrane and be relatively unsusceptible to multidrug efflux pumps.

Researchers have identified a few compounds with antibacterial activity that target lipid A biosynthesis. WO 97/42179 to Patchett et al. discloses compounds of the formula:

The compounds possess activity against certain gram-negative organisms, for example Escherichia coli, but are not active against other medically important gram-negative bacteria, for example Pseudomonas aeruginosa. Subsequent studies have found that the primary reason for their inactivity against particular, medically important gram-negative bacteria is their poor ability to inhibit P. aeruginosa LpxC; efflux by the major multidrug efflux pump or inability to penetrate the outer membrane were not the critical factors.

Jackman et al., in J. Biol. Chem. (vol. 275, no. 15, Apr. 14, 2000, pps. 11002-11009), discuss the mechanism of lipid A biosynthesis in the context of gram-negative bacteria and discloses a new class of hydroxamate-containing inhibitors of LpxC. Wyckoff et al., in Trends in Microbiology (vol. 6, no. 4, April 1998, pps. 154-159), discuss the role of LpxC in lipid A biosynthesis and its role in regulation. Wyckoff et al. disclose a few oxazoline hydroxamic acids that inhibit bacterial growth. However, Wyckoff et al. also discuss the shortcomings of the available deacetylase inhibitors as bactericidal agents against Pseudomonas and that more work is needed to be done in the area.

Thus, an increasing need exists for LpxC inhibitors that have activity as bactericidal agents against gram-negative bacteria. It is, accordingly, an object of this invention to provide compounds and combinations of such compounds for use in the preparation of antibacterials and other pharmaceuticals capable of inhibiting Gram-negative bacterial infections.

U.S. Patent Publication No. 2001/0053555 (U.S. patent application Ser. No. 08/958,638) published Dec. 20, 2001, corresponding to WO 98/18754 published May 7, 1998 discloses a combinatorial library of hydroxylamine, hydroxamic acid, hydroxyurea and hydroxylsulfonamide compounds purported to be potentially useful as inhibitors of metalloproteases. U.S. Pat. No. 6,281,245, a continuation in part of U.S. Ser. No. 08/958,638 claims a method of inhibiting a deformylase enzyme by administering one of the hydroxylamine compounds from the combinatorial library as disclosed in U.S. Patent Publication No. 2001/0053555 and the corresponding WO 98/18754. Related to the above disclosed patent publications is WO 99/57097, published Nov. 11, 1999, that discloses a method of solid phase synthesis of the hydroxylamine library of compounds. WO 00/61134 (to British Biotech Pharmaceuticals Limited), published Oct. 19, 2000, discloses compounds of the formula below:

The compounds are useful as antimicrobial agents that are believed to have bactericidal activity at least in part to intracellular inhibition of bacterial polypeptide deformylase.

In an earlier to British Biotech Pharmaceuticals Limited, WO 99/39704, published Aug. 12, 1999, compounds of the formula below are disclosed:

The compounds are useful as antimicrobial agents useful against gram-negative and gram positive bacteria.

Recently, De Novo Pharmaceuticals LTD disclosed in WO 02/50081, published Jun. 27, 2002, antibacterial and antiprotozoal agents having the formulae shown below:

The patent publication discusses that the antibacterial activity is due, at least in part, to intracellular inhibition of bacterial polypeptide deformylase.

SUMMARY OF THE INVENTION

The present invention provides novel compounds, pharmaceutical formulations including the compounds, methods of inhibiting UDP-3-O—(R-3-hydroxydecanoyl)-N-acetylglucosamine deacetylase (LpxC), and methods of treating gram-negative bacterial infections.

In one embodiment, the present invention provides compounds of formula I:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted C₂-C₆-alkenyl,     -   (4) substituted or unsubstituted C₂-C₆-alkynyl,     -   (5) substituted or unsubstituted aryl,     -   (6) substituted or unsubstituted heterocyclyl, and     -   (7) substituted or unsubstituted heteroaryl;         L is absent or selected from the group consisting of     -   (1) substituted or unsubstituted C₁-C₆-alkyl,     -   (2) —(NH)₀₋₁—(CH₂)_(j)—NR^(3L)—(CH₂)_(k)—,     -   (3) —(NH)₀₋₁—C(R^(1L), R^(2L))—NR^(3L)—C(R^(1L), R^(2L))—,     -   (4) —C(R^(1L), R^(2L))—O—C(R^(1L), R^(2L))—,     -   (5) —(CH₂)_(j)—NR^(3L)—C(R^(1L), R^(2L))—CONH—(CH₂)_(k)—,     -   (6) —CO—C(R^(1L), R^(2L))—NHCO—,     -   (7) —CONH—,     -   (8) —NHCO—,     -   wherein     -   R^(1L), R^(2L), and R^(3L) are independently selected from the         group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) C₁-C₆-alkyl substituted with aryl,         -   (d) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (e) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S;     -   j is an integer of 0-4;     -   k is an integer of 0-4;         D is absent or selected from the group consisting of     -   (1) substituted or unsubstituted C₃-C₈-cycloalkyl,     -   (2) substituted or unsubstituted aryl,     -   (3) substituted or unsubstituted heterocyclyl, and     -   (4) substituted or unsubstituted heteroaryl;         G is absent or selected from the group consisting of     -   (1) —(CH₂)_(i)—O—(CH₂)_(i)—,     -   (2) —(CH₂)_(i)—S—(CH₂)_(i)—,     -   (3) —(CH₂)_(i)—NR^(g)-—(CH₂)_(i)—,     -   (4) —C(═O)—,     -   (5) —NHC(═O)—,     -   (6) —C(═O)NH—,     -   (7) —(CH₂)_(i)NHCH₂C(═O)NH—,     -   (8) —C≡C—,     -   (9) —C≡C—C≡C—, and     -   (10) —C═C—;     -   wherein     -   Rg is H or substituted or unsubstituted C₁-C₆-alkyl;     -   i is an interger of 0-4;         Y is selected from the group consisting of     -   (1) substituted or unsubstituted C₃-C₈-cycloalkyl,     -   (2) substituted or unsubstituted aryl,     -   (3) substituted or unsubstituted heterocyclyl, and     -   (4) substituted or unsubstituted heteroaryl;         X is selected from the group consisting of     -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-(C═O)—,     -   (3) —C₂-C₆-alkenyl-(C═O)—,     -   (4) —C₂-C₆-alkynyl-(C═O)—, and     -   (5) —CH₂—;     -   or when B is absent, X and A, together with the atoms to which         they are attached can form a heterocyclic ring, having from 5 to         8 ring atoms, wherein 1-2 ring atoms of the heterocyclic ring         system are selected from N, O and S;         B is a absent or

-   -   wherein R^(1b) and R^(2b), are independently selected from the         group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) substituted or unsubstituted C₂-C₆-alkenyl,         -   (d) substituted or unsubstituted C₂-C₆-alkynyl,         -   (e) substituted or unsubstituted aryl,         -   (f) substituted or unsubstituted heterocyclyl,         -   (g) substituted or unsubstituted heteroaryl,         -   (h) C₁-C₆-alkyl substituted with aryl,         -   (i) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (j) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1b) and R^(2b), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 5 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S;

q is an integer of 0-4;

R₃ is H or substituted or unsubstituted C₁-C₆-alkyl,

-   -   or R₃ and A, together with the atoms to which they are attached         can form a substituted or unsubstituted 3-10 membered cycloalkyl         or a heterocyclic ring system, wherein the heterocyclic ring         system may have from 3 to 10 ring atoms, with 1 to 2 rings being         in the ring system and contain from 1-4 heteroatoms selected         from N, O and S;         R⁴ is H or substituted or unsubstituted C₁-C₆-alkyl,     -   or R⁴ and A, together with the atoms to which they are attached         can form a substituted or unsubstituted heterocyclic ring,         having from 3 to 8 ring atoms, wherein 1-2 ring atoms of the         heterocyclic ring system are selected from N, O and S;         n is an integer of 0-6;         A is selected from the group consisting of     -   (1) H,     -   (2) —(CH₂)_(r)C(R^(1a), R^(2a))(CH₂)_(s)OR^(3a),     -   (3) —(CH₂)_(r)C(R^(1a), R^(2a))N(R^(4a), R^(1a)),     -   (4) —(CH₂)_(r)C(R^(1a), R^(2a))N(R^(4a))COR^(3a),     -   (5) —(CH₂)_(r)C(R^(1a), R^(2a))NHCON(R^(4a), R^(1a)),     -   (6) —(CH₂)_(r)C(R^(1a), R^(2a))NHC(═NH)N(R^(4a), R^(5a)),     -   (7) —CH(R^(1a), R^(2a)),     -   (8) —C≡CH,     -   (9) —(CH₂)_(r)C(R^(1a), R^(2a))CN,     -   (10) —(CH₂)_(r)C(R^(1a), R^(2a))CO₂R^(3a), and     -   (11) —(CH₂)_(r)C(R^(1a), R^(2a))CON(R^(4a), R^(5a)),     -   wherein R^(1a), R^(2a), R^(3a), R^(4a), and R^(5a) are         independently selected from the group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) substituted or unsubstituted aryl,         -   (d) substituted or unsubstituted heterocyclyl,         -   (e) substituted or unsubstituted heteroaryl,         -   (f) C₁-C₆-alkyl substituted with aryl,         -   (g) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (h) C₁-C₆-alkyl substituted with heteroaryl,         -   or R^(4a) and R^(5a) together with the N atom to which they             are attached can form a substituted or unsubstituted             heterocyclic ring, having from 5 to 8 ring atoms, wherein             1-2 ring atoms of the heterocyclic ring system are selected             from N, O and S;     -   r is an integer of 0-4;     -   s is an integer of 0-4;         Q is absent or selected from the group consisting of     -   (1) —C(═O)N(R₁, R₂),     -   (2) —NHC(═O)N(R₁, R₂),     -   (3) —N(OH)C(═O)N(R₁, R₂),     -   (4) —CH(OH)C(═O)N(R₁, R₂),     -   (5) —CH[N(R^(2q), R^(3q))]C(═O)N(R₁, R₂),     -   (6) —CHR_(1q)C(═O)N(R₁, R₂),     -   (7) —CO₂H,     -   (8) —C(═O)NHSO₂R^(4q),     -   (9) —SO₂NH₂,     -   (10) —N(OH)C(═O)R^(1q),     -   (11) —N(OH)SO₂R^(4q),     -   (12) —NHSO₂R^(4q),     -   (13) —SH,     -   (14) —CH(SH)(CH₂)₀₋₁C(═O)N(R₁, R₂),     -   (15) —CH(SH)(CH₂)₀₋₁CO₂H,     -   (16) —CH(OH)(CH₂)₀₋₁CO₂H,     -   (17) —CH(SH)CH₂CO₂R^(1q),     -   (18) —CH(OH)(CH₂)SO₂NH₂,     -   (19) CH(CH₂SH)NHCOR^(1q),     -   (20) —CH(CH₂SH)NHSO₂R^(4q),     -   (21) —CH(CH₂SR^(5q))CO₂H,     -   (22) —CH(CH₂SH)NHSO₂NH₂,     -   (23) —CH(CH₂OH)CO₂H,     -   (24) —CH(CH₂OH)NHSO₂NH₂,     -   (25) —C(═O)CH₂CO₂H,     -   (26) —C(═O)(CH₂)₀₋₁CONH₂,     -   (27) —OS₂NHR^(5q),     -   (28) —SO₂NHNH₂,     -   (29) —P(═O)(OH)₂,     -   (30)

-   -   (31)

-   -   (32)

-   -   wherein     -   R₁, is selected from the group consisting of         -   (1) H,         -   (2) —OH,         -   (3) —OC₁₋₆-alkyl,         -   (4) —N(R^(2q), R^(3q)), and         -   (5) substituted or unsubstituted C₁₋₆-alkyl;     -   R₂ is selected from the group consisting of         -   (1) H,         -   (2) substituted or unsubstituted C₁-C₆-alkyl,         -   (3) substituted or unsubstituted C₂-C₆-alkenyl,         -   (4) substituted or unsubstituted C₂-C₆-alkenyl,         -   (5) substituted or unsubstituted aryl,         -   (6) substituted or unsubstituted heterocyclyl,         -   (7) substituted or unsubstituted heteroaryl,         -   (8) C₁-C₆-alkyl substituted with aryl,         -   (9) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (10) C₁-C₆-alkyl substituted with heteroaryl,         -   or R¹ and R², together with the N atom to which they are             attached can form a substituted or unsubstituted             heterocyclic ring, having from 3 to 10 ring atoms, wherein             1-4 ring atoms of the heterocyclic ring system are selected             from N, O and S,         -   or R² and R⁴, together with the N atoms to which they are             attached can form a substituted or unsubstituted             heterocyclic ring, having from 3 to 10 ring atoms, wherein             1-4 ring atoms of the heterocyclic ring system are selected             from N, O and S;     -   R^(1q), R^(2q), R^(3q), R^(4q), and R^(5q) are selected from H         or C₁-C₆ alkyl,         wherein B is absent, or E, L, G, and B are absent, or E, L, and         G are absent, or E, L, and B are absent, or E, L, D, G, and B         are absent.

In one aspect, the invention provides a method of inhibiting a deacetylase enzyme in a gram-negative bacteria, thereby affecting bacterial growth, comprising administering to a patient in need of such inhibition a compound of formula I.

In another aspect, the invention provides a method of inhibiting LpxC, thereby modulating the virulence of a bacterial infection, comprising administering to a patient in need of such inhibition a compound of formula I.

In another aspect, the invention provides a method for treating a subject with a gram-negative bacterial infection comprising administering to the subject in need thereof an antibacterially effective amount of a compound of formula I with a pharmaceutically acceptable carrier. In a preferred embodiment of the method of treatment, the subject is a mammal and in some embodiments, a human.

In another aspect, the invention provides a method of administering an inhibitory amount of a compound of formula I to fermentative or non-fermentative gram-negative bacteria. In a preferred embodiment of the method of administering an inhibitory amount of a compound of formula I to fermentative or non-fermentative gram-negative bacteria, the gram-negative bacteria are selected from the group consisting of Pseudomonas aeruginosa, Stenotrophomonas maltophila, Burkholderia cepacia, Alcaligenes xylosoxidans, Acinetobacter, Enterobacteriaceae, Haemophilus, and Neisseria species.

In another embodiment, the invention provides a method of administering an inhibitory amount of a compound of formula I to gram-negative bacteria, such as Enterobacteriaceae which is selected from the group consisting of organisms such as Serratia, Proteus, Klebsiella, Enterobacter, Citrobacter, Salmonella, Providencia, Morganella, Cedecea, and Edwardsiella species and Escherichia coli.

Another embodiment of the invention provides a pharmaceutical composition comprising an effective amount of a compound of Formula I with a pharmaceutically acceptable carrier thereof.

Pharmaceutical formulations according to the present invention are provided which include any of the compounds described above in combination with a pharmaceutically acceptable carrier.

Another embodiment of the invention provides a method of co-administering the compound of formula I with other therapeutic agents that are selected for their particular usefulness against the condition that is being treated.

For example, the compound of formula I is useful in combination with other anti-bacterial agents. The compound of formula I augments the sensitivity of gram-negative bacteria to existing classes of antibacterials. Combinations of the presently disclosed compounds with other anti-bacterial agents are within the scope of the invention. Such anti-bacterial agents include, but are not limited to, erythromycin, rifampicin, Nalidixic acid, carbenicillin, bacitracin, cycloserine, fosfomycin, and vancomycin.

DETAILED DESCRIPTION

The present invention provides novel compounds, methods for inhibiting LpxC in gram-negative bacteria, and novel methods for treating bacterial infections. The compounds provided herein can be formulated into pharmaceutical formulations and medicaments that are useful in the methods of the invention. The invention also provides for the use of the compounds in preparing medicaments and pharmaceutical formulations, for use of the compounds in inhibiting LpxC, and for use of the compounds in treating bacterial infections in a subject.

The following abbreviations and definitions are used throughout this application:

“LpxC” is an abbreviation that stands for UDP-3-O—(R-3-hydroxydecanoyl)-N-acetylglucosamine deacetylase.

Generally, reference to a certain element such as hydrogen or H is meant to include all isotopes of that element. For example, if an R group is defined to include hydrogen or H, it also includes deuterium and tritium.

The phrase “alkyl” refers to alkyl groups that do not contain heteroatoms. Thus the phrase includes straight chain alkyl groups such as methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl and the like. The phrase also includes branched chain isomers of straight chain alkyl groups, including but not limited to, the following that are provided by way of example: —CH(CH₃)₂, —CH(CH₃)(CH₂CH₃), —CH(CH₂CH₃)₂, —C(CH₃)₃, —C(CH₂CH₃)₃, —CH₂CH(CH₃)₂, —CH₂CH(CH₃)(CH₂CH₃), —CH₂CH(CH₂CH₃)₂, —CH₂C(CH₃)₃, —CH₂C(CH₂CH₃)₃, —CH(CH₃)CH(CH₃)(CH₂CH₃), —CH₂CH₂CH(CH₃)₂, —CH₂CH₂CH(CH₃)(CH₂CH₃), —CH₂CH₂CH(CH₂CH₃)₂, —CH₂CH₂C(CH₃)₃, —CH₂CH₂C(CH₂CH₃)₃, —CH(CH₃)CH₂CH(CH₃)₂, —CH(CH₃)CH(CH₃)CH(CH₃)₂, —CH(CH₂CH₃)CH(CH₃)CH(CH₃)(CH₂CH₃), and others. The phrase also includes cyclic alkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl and such rings substituted with straight and branched chain alkyl groups as defined above. Thus the phrase alkyl groups includes primary alkyl groups, secondary alkyl groups, and tertiary alkyl groups. Preferred alkyl groups include straight and branched chain alkyl groups and cyclic alkyl groups having 1 to 12 carbon atoms.

The phrase “substituted alkyl” refers to an alkyl group as defined above in which one or more bonds to a carbon(s) or hydrogen(s) are replaced by a bond to non-hydrogen and non-carbon atoms such as, but not limited to, a halogen atom such as F, Cl, Br, and I; an oxygen atom in groups such as hydroxyl groups, alkoxy groups, aryloxy groups, and ester groups; a sulfur atom in groups such as thiol groups, alkyl and aryl sulfide groups, sulfone groups, sulfonyl groups, and sulfoxide groups; a nitrogen atom in groups such as amines, amides, alkylamines, dialkylamines, arylamines, alkylarylamines, diarylamines, N-oxides, imides, and enamines; a silicon atom in groups such as in trialkylsilyl groups, dialkylarylsilyl groups, alkyldiarylsilyl groups, and triarylsilyl groups; and other heteroatoms in various other groups. Substituted alkyl groups also include groups in which one or more bonds to a carbon(s) or hydrogen(s) atom is replaced by a higher-order bond (e.g., a double- or triple-bond) to a heteroatom such as oxygen in oxo, carbonyl, carboxyl, and ester groups; nitrogen in groups such as imines, oximes, hydrazones, and nitriles. Substituted alkyl groups further include alkyl groups in which one or more bonds to a carbon(s) or hydrogen(s) atoms is replaced by a bond to an aryl, heterocyclyl group, or cycloalkyl group. Preferred substituted alkyl groups include, among others, alkyl groups in which one or more bonds to a carbon or hydrogen atom is/are replaced by one or more bonds to fluorine atoms. Another preferred substituted alkyl group is the trifluoromethyl group and other alkyl groups that contain the trifluoromethyl group. Other preferred substituted alkyl groups include those in which one or more bonds to a carbon or hydrogen atom is replaced by a bond to an oxygen atom such that the substituted alkyl group contains a hydroxyl, alkoxy, or aryloxy group. Still other preferred substituted alkyl groups include alkyl groups that have an amine, or a substituted or unsubstituted alkylamine, dialkylamine, arylamine, (alkyl)(aryl)amine, diarylamine, heterocyclylamine, diheterocyclylamine, (alkyl)(heterocyclyl)amine, or (aryl)(heterocyclyl)amine group.

The phrase “alkenyl” refers to straight and branched chain and cyclic groups such as those described with respect to alkyl groups as defined above, except that at least one double bond exists between two carbon atoms. Examples include, but are not limited to vinyl, —CH═C(H)(CH₃), —CH═C(CH₃)₂, —C(CH₃)═C(H)₂, —C(CH₃)═C(H)(CH₃), —C(CH₂CH₃)═CH₂, cyclohexenyl, cyclopentenyl, cyclohexadienyl, butadienyl, pentadienyl, and hexadienyl among others. The phrase “substituted alkenyl” has the same meaning with respect to alkenyl groups that substituted alkyl groups had with respect to unsubstituted alkyl groups. A substituted alkenyl group includes alkenyl groups in which a non-carbon or non-hydrogen atom is bonded to a carbon double bonded to another carbon and those in which one of the non-carbon or non-hydrogen atoms is bonded to a carbon not involved in a double bond to another carbon.

The phrase “alkynyl” refers to straight and branched chain groups such as those described with respect to alkyl groups as defined above, except that at least one triple bond exists between two carbon atoms. Examples include, but are not limited to —C≡C(H), —C≡C(CH₃), —C≡C(CH₂CH₃), —C(H₂)C≡C(H), —C(H)₂C≡C(CH₃), and —C(H)₂C≡C(CH₂CH₃) among others. The phrase “substituted alkynyl” has the same meaning with respect to alkynyl groups that substituted alkyl groups had with respect to unsubstituted alkyl groups. A substituted alkynyl group includes alkynyl groups in which a non-carbon or non-hydrogen atom is bonded to a carbon triple bonded to another carbon and those in which a non-carbon or non-hydrogen atom is bonded to a carbon not involved in a triple bond to another carbon.

The phrase “heterocyclyl” refers to both aromatic and nonaromatic ring compounds including monocyclic, bicyclic, and polycyclic ring compounds such as, but not limited to, quinuclidinyl, containing 3 or more ring members of which one or more is a heteroatom such as, but not limited to, N, O, and S. Although the phrase “unsubstituted heterocyclyl” includes condensed heterocyclic rings such as benzimidazolyl, it does not include heterocyclyl groups that have other groups such as alkyl or halo groups bonded to one of the ring members as compounds such as 2-methylbenzimidazolyl are substituted heterocyclyl groups. Examples of heterocyclyl groups include, but are not limited to: unsaturated 3 to 8 membered rings containing 1 to 4 nitrogen atoms such as, but not limited to pyrrolyl, pyrrolinyl, imidazolyl, pyrazolyl, pyridyl, dihydropyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazolyl (e.g. 4H-1,2,4-triazolyl, 1H-1,2,3-triazolyl, 2H-1,2,3-triazolyl etc.), tetrazolyl, (e.g. 1H-tetrazolyl, 2H tetrazolyl, etc.); saturated 3 to 8 membered rings containing 1 to 4 nitrogen atoms such as, but not limited to, pyrrolidinyl, imidazolidinyl, piperidinyl, piperazinyl; condensed unsaturated heterocyclic groups containing 1 to 4 nitrogen atoms such as, but not limited to, indolyl, isoindolyl, indolinyl, indolizinyl, benzimidazolyl, quinolyl, isoquinolyl, indazolyl, benzotriazolyl; unsaturated 3 to 8 membered rings containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms such as, but not limited to, oxazolyl, isoxazolyl, oxadiazolyl (e.g. 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, etc.); saturated 3 to 8 membered rings containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms such as, but not limited to, morpholinyl; unsaturated condensed heterocyclic groups containing 1 to 2 oxygen atoms and 1 to 3 nitrogen atoms, for example, benzoxazolyl, benzoxadiazolyl, benzoxazinyl (e.g. 2H-1,4-benzoxazinyl etc.); unsaturated 3 to 8 membered rings containing 1 to 3 sulfur atoms and 1 to 3 nitrogen atoms such as, but not limited to, thiazolyl, isothiazolyl, thiadiazolyl (e.g. 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, etc.); saturated 3 to 8 membered rings containing 1 to 2 sulfur atoms and 1 to 3 nitrogen atoms such as, but not limited to, thiazolodinyl; saturated and unsaturated 3 to 8 membered rings containing 1 to 2 sulfur atoms such as, but not limited to, thienyl, dihydrodithiinyl, dihydrodithionyl, tetrahydrothiophene, tetrahydrothiopyran; unsaturated condensed heterocyclic rings containing 1 to 2 sulfur atoms and 1 to 3 nitrogen atoms such as, but not limited to, benzothiazolyl, benzothiadiazolyl, benzothiazinyl (e.g. 2H-1,4-benzothiazinyl, etc.), dihydrobenzothiazinyl (e.g. 2H-3,4-dihydrobenzothiazinyl, etc.), unsaturated 3 to 8 membered rings containing oxygen atoms such as, but not limited to furyl; unsaturated condensed heterocyclic rings containing 1 to 2 oxygen atoms such as benzodioxolyl (e.g. 1,3-benzodioxoyl, etc.); unsaturated 3 to 8 membered rings containing an oxygen atom and 1 to 2 sulfur atoms such as, but not limited to, dihydrooxathiinyl; saturated 3 to 8 membered rings containing 1 to 2 oxygen atoms and 1 to 2 sulfur atoms such as 1,4-oxathiane; unsaturated condensed rings containing 1 to 2 sulfur atoms such as benzothienyl, benzodithiinyl; and unsaturated condensed heterocyclic rings containing an oxygen atom and 1 to 2 oxygen atoms such as benzoxathiinyl. Heterocyclyl group also include those described above in which one or more S atoms in the ring is double-bonded to one or two oxygen atoms (sulfoxides and sulfones). For example, heterocyclyl groups include tetrahydrothiophene, tetrahydrothiophene oxide, and tetrahydrothiophene 1,1-dioxide. Preferred heterocyclyl groups contain 5 or 6 ring members. More preferred heterocyclyl groups include morpholine, piperazine, piperidine, pyrrolidine, imidazole, pyrazole, 1,2,3-triazole, 1,2,4-triazole, tetrazole, thiomorpholine, thiomorpholine in which the S atom of the thiomorpholine is bonded to one or more O atoms, pyrrole, homopiperazine, oxazolidin-2-one, pyrrolidin-2-one, oxazole, quinuclidine, thiazole, isoxazole, furan, and tetrahydrofuran.

The phrase “substituted heterocyclyl” refers to a heterocyclyl group as defined above in which one of the ring members is bonded to a non-hydrogen atom such as described above with respect to substituted alkyl groups and substituted aryl groups. Examples, include, but are not limited to, 2-methylbenzimidazolyl, 5-methylbenzimidazolyl, 5-chlorobenzthiazolyl, 1-methyl piperazinyl, and 2-chloropyridyl among others.

The phrase “aryl” refers to aryl groups that do not contain heteroatoms. Thus the phrase includes, but is not limited to, groups such as phenyl, biphenyl, anthracenyl, naphthenyl by way of example. Although the phrase “unsubstituted aryl” includes groups containing condensed rings such as naphthalene, it does not include aryl groups that have other groups such as alkyl or halo groups bonded to one of the ring members, as aryl groups such as tolyl are considered herein to be substituted aryl groups as described below. A preferred unsubstituted aryl group is phenyl. Unsubstituted aryl groups may be bonded to one or more carbon atom(s), oxygen atom(s), nitrogen atom(s), and/or sulfur atom(s) in the parent compound, however.

The phrase “substituted aryl group” has the same meaning with respect to unsubstituted aryl groups that substituted alkyl groups had with respect to unsubstituted alkyl groups. However, a substituted aryl group also includes aryl groups in which one of the aromatic carbons is bonded to one of the non-carbon or non-hydrogen atoms described above and also includes aryl groups in which one or more aromatic carbons of the aryl group is bonded to a substituted and/or unsubstituted alkyl, alkenyl, or alkynyl group as defined herein. This includes bonding arrangements in which two carbon atoms of an aryl group are bonded to two atoms of an alkyl, alkenyl, or alkynyl group to define a fused ring system (e.g. dihydronaphthyl or tetrahydronaphthyl). Thus, the phrase “substituted aryl” includes, but is not limited to tolyl, and hydroxyphenyl among others. Preferred substituents include straight and branched chain alkyl groups, —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, —NHCOCH₃.

The term “heteroaryl”, as used herein, refers to a cyclic or bicyclic aromatic radical having from five to ten ring atoms in each ring of which one atom of the cyclic or bicyclic ring is selected from S, O and N; zero, one or two ring atoms are additional heteroatoms independently selected from S, O and N; and the remaining ring atoms are carbon, the radical being joined to the rest of the molecule via any of the ring atoms, such as, for example, pyridyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, and naphthyridinyl, and the like.

The term “substituted heteroaryl” as used herein refers to a heteroaryl group as defined herein substituted by independent replacement of one, two or three of the hydrogen atoms thereon with Cl, Br, F, I, OH, CN, C₁-C₃-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkoxy substituted with aryl, haloalkyl, thioalkoxy, amino, alkylamino, dialkylamino, mercapto, nitro, carboxaldehyde, carboxy, alkoxycarbonyl and carboxamide. In addition, any one substituent may be an aryl, heteroaryl, or heterocycloalkyl group. Preferred substituents include straight and branched chain alkyl groups, —CH₃, —C₂HS, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, —NHCOCH₃.

The term “biaryl” refers to a group or substituent to which two aryl groups, which are not condensed to each other, are bound. Exemplary biaryl compounds include, for example, phenylbenzene, diphenyldiazene, 4-methylthio-1-phenylbenzene, phenoxybenzene, (2-phenylethynyl)benzene, diphenyl ketone, (4-phenylbuta-1,3-diynyl)benzene, phenylbenzylamine, (phenylmethoxy)benzene, and the like. Preferred optionally substituted biaryl groups include: 2-(phenylamino)-N-[4-(2-phenylethynyl)phenyl]acetamide, 1,4-diphenylbenzene, N-[4-(2-phenylethynyl)phenyl]-2-[benzylamino]acetamide, 2-amino-N-[4-(2-phenylethynyl)phenyl]propanamide, 2-amino-N-[4-(2-phenylethynyl)phenyl]acetamide, 2-(cyclopropylamino)-N-[4-(2-phenylethynyl)phenyl]acetamide, 2-(ethylamino)-N-[4-(2-phenylethynyl)phenyl]acetamide, 2-[(2-methylpropyl)amino]-N-[4-(2-phenylethynyl)phenyl]acetamide, 5-phenyl-2H-benzo[d]1,3-dioxolene, 2-chloro-1-methoxy-4-phenylbenzene, 2-[(imidazolylmethyl)amino]-N-[4-(2-phenylethynyl)phenyl]acetamide, 4-phenyl-1-phenoxybenzene, N-(2-aminoethyl)[4-(2-phenylethynyl)phenyl]carboxamide, 2-{[(4-fluorophenyl)methyl]amino-}N-[4-(2-phenylethynyl)phenyl]acetamide, 2-{[(4-methylphenyl)methyl]amino}-N-[4-(2-phenylethynyl)phenyl]acetamide, 4-phenyl-1-(trifluoromethyl)benzene, 1-butyl-4-phenylbenzene, 2-(cyclohexylamino)-N-[4-(2-phenylethynyl)phenyl]acetamide, 2-(ethylmethylamino)-N-[4-(2-phenylethynyl)phenyl]acetamide, 2-(butylamino)-N-[4-(2-phenylethynyl)phenyl]acetamide, N-[4-(2-phenylethynyl)phenyl]-2-(4-pyridylamino)acetamide, N-[4-(2-phenylethynyl)phenyl]-2-(quinuclidin-3-ylamino)acetamide, N-[4-(2-phenylethynyl)phenyl]pyrrolidin-2-ylcarboxamide, 2-amino-3-methyl-N-[4-(2-phenylethynyl)phenyl]butanamide, 4-(4-phenylbuta-1,3-diynyl)phenylamine, 2-(dimethylamino)-N-[4-(4-phenylbuta-1,3-diynyl)phenyl]acetamide, 2-(ethylamino)-N-[4-(4-phenylbuta-1,3-diynyl)phenyl]acetamide, 4-ethyl-1-phenylbenzene, 1-[4-(2-phenylethynyl)phenyl]ethan-1-one, N-(1-carbamoyl-2-hydroxypropyl)[4-(4-phenylbuta-1,3-diynyl)phenyl]carboxamide, N-[4-(2-phenylethynyl)phenyl]propanamide, 4-methoxyphenyl phenyl ketone, phenyl-N-benzamide, (tert-butoxy)-N-[(4-phenylphenyl)methyl]carboxamide, 2-(3-phenylphenoxy)ethanehydroxamic acid, 3-phenylphenyl propanoate, 1-(4-ethoxyphenyl)-4-methoxybenzene, and [4-(2-phenylethynyl)phenyl]pyrrole.

The term “heteroarylaryl” refers to a biaryl group where one of the aryl groups is a heteroaryl group. Exemplary heteroarylaryl groups include, for example, 2-phenylpyridine, phenylpyrrole, 3-(2-phenylethynyl)pyridine, phenylpyrazole, 5-(2-phenylethynyl)-1,3-dihydropyrimidine-2,4-dione, 4-phenyl-1,2,3-thiadiazole, 2-(2-phenylethynyl)pyrazine, 2-phenylthiophene, phenylimidazole, 3-(2-piperazinylphenyl)furan, 3-(2,4-dichlorophenyl)-4-methylpyrrole, and the like. Preferred optionally substituted heteroarylaryl groups include: 5-(2-phenylethynyl)pyrimidine-2-ylamine, 1-methoxy-4-(2-thienyl)benzene, 1-methoxy-3-(2-thienyl)benzene, 5-methyl-2-phenylpyridine, 5-methyl-3-phenylisoxazole, 2-[3-(trifluoromethyl)phenyl]furan, 3-fluoro-5-(2-furyl)-2-methoxy-1-prop-2-enylbenzene, (hydroxyimino)(5-phenyl(2-thienyl))methane, 5-[(4-methylpiperazinyl)methyl]-2-phenylthiophene, 2-(4-ethylphenyl)thiophene, 4-methylthio-1-(2-thienyl)benzene, 2-(3-nitrophenyl)thiophene, (tert-butoxy)-N-[(5-phenyl(3-pyridyl))methyl]carboxamide, hydroxy-N-[(5-phenyl(3-pyridyl))methyl]amide, 2-(phenylmethylthio)pyridine, and benzylimidazole.

The term “heteroarylheteroaryl” refers to a biaryl group where both of the aryl groups is a heteroaryl group. Exemplary heteroarylheteroaryl groups include, for example, 3-pyridylimidazole, 2-imidazolylpyrazine, and the like. Preferred optionally substituted heteroarylheteroaryl groups include: 2-(4-piperazinyl-3-pyridyl)furan, diethyl(3-pyrazin-2-yl(4-pyridyl))amine, and dimethyl {2-[2-(5-methylpyrazin-2-yl)ethynyl] (4-pyridyl)}amine.

“Optionally substituted” refers to the optional replacement of hydrogen with one or more monovalent or divalent radicals. Optionally substituted groups include those described herein, for each group in which a distinct definition for substitution is supplied. Additionally, suitable substitution groups include, for example, hydroxyl, nitro, amino, imino, cyano, halo, thio, thioamido, amidino, imidino, oxo, oxamidino, methoxamidino, imidino, guanidino, sulfonamido, carboxyl, formyl, alkyl, substituted alkyl, haloloweralkyl, loweralkoxy, haloloweralkoxy, loweralkoxyalkyl, alkylcarbonyl, arylcarbonyl, aralkylcarbonyl, heteroarylcarbonyl, heteroaralkylcarbonyl, alkylthio, aminoalkyl, cyanoalkyl, benzyl, pyridyl, pyrazolyl, pyrrole, thiophene, imidazolyl, and the like.

Representative substituted amidino and heterocycloamidino groups include, for example, those shown below. These amidino and heterocycloamidino groups can be further substituted as will be apparent to those having skill in the organic and medicinal chemistry arts in conjunction with the disclosure herein.

Representative substituted alkylcarbonylamino, alkyloxycarbonylamino, aminoalkyloxycarbonylamino, and arylcarbonylamino groups include, for example, those shown below. These groups can be further substituted as will be apparent to those having skill in the organic and medicinal chemistry arts in conjunction with the disclosure herein.

Representative substituted aminocarbonyl groups include, for example, those shown below. These can be further substituted by heterocyclo groups and heteroaryl groups as will be apparent to those having skill in the organic and medicinal chemistry arts in conjunction with the disclosure herein. Preferred aminocarbonyl groups include: N-(2-cyanoethyl)carboxamide, N-(3-methoxypropyl)carboxamide, N-cyclopropylcarboxamide, N-(2-hydroxy-isopropyl)carboxamide, methyl 2-carbonylamino-3-hydroxypropanoate, N-(2-hydroxypropyl)carboxamide, N-(2-hydroxy-isopropyl)carboxamide, N-[2-hydroxy-1-(hydroxymethyl)ethyl]carboxamide, N-(2-carbonylaminoethyl)acetamide, N-(2-(2-pyridyl)ethyl)carboxamide, N-(2-pyridylmethyl)carboxamide, N-(oxolan-2-ylmethyl)carboxaamide, N-(4-hydroxypyrrolidin-2-yl)carboxamide, N-[2-(2-hydroxyethoxy)ethyl]carboxamide, N-(4-hydroxycyclohexyl)carboxamide, N-[2-(2-oxo-4-imidazolinyl)ethyl]carboxamide, N-(carbonylaminomethyl)acetamide, N-(3-pyrrolidinylpropyl)carboxamide, N-[1-(carbonylaminomethyl)pyrrolidin-3-yl]acetamide, N-(2-morpholin-4-ylethyl)carboxamide, N-[3-(2-oxopyrrolidinyl)propyl]carboxamide, 4-methyl-2-oxopiperazinecarbaldehyde, N-(2-hydroxy-3-pyrrolidinylpropyl)carboxamide, N-(2-hydroxy-3-morpholin-4-ylpropyl)carboxamide, N-{2-[(5-cyano-2-pyridyl)amino]ethyl}carboxamide, 3-(dimethylamino)pyrrolidinecarbaldehyde, N-[(5-methylpyrazin-2-yl)methyl]carboxamide, 2,2,2-trifluoro-N-(1-formylpyrrolidin-3-yl)acetamide,

Representative substituted alkoxycarbonyl groups include, for example, those shown below. These alkoxycarbonyl groups can be further substituted as will be apparent to those having skill in the organic and medicinal chemistry arts in conjunction with the disclosure herein.

The term “protected” with respect to hydroxyl groups, amine groups, and sulfhydryl groups refers to forms of these functionalities that are protected from undesirable reaction with a protecting group known to those skilled in the art such as those set forth in Protective Groups in Organic Synthesis, Greene, T. W.; Wuts, P. G. M., John Wiley & Sons, New York, N.Y., (3rd Edition, 1999) that can be added or removed using the procedures set forth therein. Examples of protected hydroxyl groups include, but are not limited to, silyl ethers such as those obtained by reaction of a hydroxyl group with a reagent such as, but not limited to, t-butyldimethyl-chlorosilane, trimethylehlorosilane, triisopropylchlorosilane, triethylchlorosilane; substituted methyl and ethyl ethers such as, but not limited to methoxymethyl ether, methylhiomethyl ether, benzyloxymethyl ether, t-butoxymethyl ether, 2-methoxyethoxymethyl ether, tetrahydropyranyl ethers, 1-ethoxyethyl ether, allyl ether, benzyl ether; esters such as, but not limited to, benzoylformate, formate, acetate, trichloroacetate, and trifluoracetate. Examples of protected amine groups include, but are not limited to, amides such as, formamide, acetamide, trifluoroacetamide, and benzamide; imides, such as phthalimide, and dithiosuccinimide; and others. Examples of protected sulfhydryl groups include, but are not limited to, thioethers such as S-benzyl thioether, and S-4-picolyl thioether; substituted S-methyl derivatives such as hemithio, dithio and aminothio acetals; and others.

A “pharmaceutically acceptable salt” includes a salt with an inorganic base, organic base, inorganic acid, organic acid, or basic or acidic amino acid. As salts of inorganic bases, the invention includes, for example, alkali metals such as sodium or potassium; alkaline earth metals such as calcium and magnesium or aluminum; and ammonia. As salts of organic bases, the invention includes, for example, trimethylamine, triethylamine, pyridine, picoline, ethanolamine, diethanolamine, and triethanolamine. As salts of inorganic acids, the instant invention includes, for example, hydrochloric acid, hydroboric acid, nitric acid, sulfuric acid, and phosphoric acid. As salts of organic acids, the instant invention includes, for example, formic acid, acetic acid, trifluoroacetic acid, fumaric acid, oxalic acid, tartaric acid, maleic acid, citric acid, succinic acid, malic acid, methanesulfonic acid, benzenesulfonic acid, and p-toluenesulfonic acid. As salts of basic amino acids, the instant invention includes, for example, arginine, lysine and ornithine. Acidic amino acids include, for example, aspartic acid and glutamic acid.

As used herein, the term “pharmaceutically acceptable ester” refers to esters that hydrolyze in vivo and include those that break down readily in the human body to leave the parent compound or a salt thereof. Suitable ester groups include, for example, those derived from pharmaceutically acceptable aliphatic carboxylic acids, particularly alkanoic, alkenoic, cycloalkanoic and alkanedioic acids, in which each alkyl or alkenyl moiety advantageously has not more than 6 carbon atoms. Representative examples of particular esters include, but are not limited to, formates, acetates, propionates, butyrates, acrylates and ethylsuccinates.

The term “pharmaceutically acceptable prodrugs” as used herein refers to those prodrugs of the compounds of the present invention that are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use, as well as the zwitterionic forms, where possible, of the compounds of the invention. The term “prodrug” refers to compounds that are rapidly transformed in vivo to yield the parent compound of the above formula, for example by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems, Vol. 14 of the A.C.S. Symposium Series, and in Edward B. Roche, ed., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference.

The term “antibacterial agent” refers to agents synthesized or modified in the laboratory that have either bactericidal or bacteriostatic activity. An “active” agent in this context will inhibit the growth of P. aeruginosa and other gram-negative bacteria. The term “inhibiting the growth” indicates that the rate of increase in the numbers of a population of a particular bacterium is reduced. Thus, the term includes situations in which the bacterial population increases but at a reduced rate, as well as situations where the growth of the population is stopped, as well as situations where the numbers of the bacteria in the population are reduced or the population even eliminated. If an enzyme activity assay is used to screen for inhibitors, one can make modifications in uptake/efflux, solubility, half-life, etc. to compounds in order to correlate enzyme inhibition with growth inhibition. The activity of antibacterial agents is not necessarily limited to bacteria but may also encompass activity against parasites, virus, and fungi.

The subject invention also includes isotopically-labeled LpxC inhibitors, that are structurally identical to those disclosed above, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. Examples of isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, sulfur, fluorine and chlorine, such as ²H, ³H, ¹³C, ¹⁴C, ¹⁵N, ¹⁸O, ¹⁷O, ³¹P, ³²P, ³⁵S, ¹⁸F and ³⁶Cl, respectively. Compounds of the present invention, prodrugs thereof, and pharmaceutically acceptable salts of said compounds and of said prodrugs that contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of this invention. Certain isotopically labeled compounds of the present invention, for example those into which radioactive isotopes such as ³H and ¹⁴C are incorporated, are useful in drug and/or substrate tissue distribution assays. Tritiated, i.e., ³H, and carbon-14, i.e., ¹⁴C, isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with heavier isotopes such as deuterium, i.e., ²H, may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements and, hence, may be preferred in some circumstances. Isotopically labeled compounds of this invention and prodrugs thereof can generally be prepared by carrying out known or referenced procedures and by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.

The present invention provides novel compounds, pharmaceutical formulations including the compounds, methods of inhibiting UDP-3-O—(R-3-hydroxydecanoyl)-N-acetylglucosamine deacetylase (LpxC), and methods of treating gram-negative bacterial infections.

In one embodiment, the present invention provides compounds of formula I:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted C₂-C₆-alkenyl,     -   (4) substituted or unsubstituted C₂-C₆-alkynyl,     -   (5) substituted or unsubstituted aryl,     -   (6) substituted or unsubstituted heterocyclyl, and     -   (7) substituted or unsubstituted heteroaryl;         L is absent or selected from the group consisting of     -   (1) substituted or unsubstituted C₁-C₆-alkyl,     -   (2) —(NH)₀₋₁—(CH₂)_(j)—NR^(3L)—(CH₂)_(k)—,     -   (3) —(NH)₀₋₁—C(R^(1L), R^(2L))—NR^(3L)—C(R^(1L), R^(2L))—,     -   (4) —C(R^(1L), R^(2L))—O—C(R^(1L), R^(2L))—,     -   (5) —(CH₂)_(j)—NR^(3L)—C(R^(1L), R^(2L))—CONH—(CH₂)_(k)—,     -   (6) CO—C(R^(1L), R^(2L))—NHCO—,     -   (7) —CONH—,     -   (8) —NHCO—,     -   wherein     -   R^(1L), R^(2L), and R^(3L) are independently selected from the         group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) C₁-C₆-alkyl substituted with aryl,         -   (d) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (e) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L) together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S,     -   j is an integer of 0-4;     -   k is an integer of 0-4;         D is absent or selected from the group consisting of     -   (1) substituted or unsubstituted C₃-C₈-cycloalkyl,     -   (2) substituted or unsubstituted aryl,     -   (3) substituted or unsubstituted heterocyclyl, and     -   (4) substituted or unsubstituted heteroaryl;         G is absent or selected from the group consisting of     -   (1) —(CH₂)_(i)—O—(CH₂)_(i)—,     -   (2) —(CH₂)_(i)—S—(CH₂)_(i)—,     -   (3) —(CH₂)_(i)—NR^(g)—(CH₂)_(i)—,     -   (4) —C(═O)—,     -   (5) —NHC(═O)—,     -   (6) —C(═O)NH—,     -   (7) —(CH₂)_(i)NHCH₂C(═O)NH—,     -   (8) —C≡C—,     -   (9) —C≡C—C≡C—, and     -   (10) —C═C—;     -   wherein     -   Rg is H or substituted or unsubstituted C₁-C₆-alkyl;     -   i is an interger of 0-4;         Y is selected from the group consisting of     -   (1) substituted or unsubstituted C₃-C₈-cycloalkyl,     -   (2) substituted or unsubstituted aryl,     -   (3) substituted or unsubstituted heterocyclyl, and     -   (4) substituted or unsubstituted heteroaryl;         X is selected from the group consisting of     -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-(C═O)—,     -   (3) —C₂-C₆-alkenyl-(C═O)—,     -   (4) —C₂-C₆-alkynyl-(C═O)—, and     -   (5) —CH₂—;     -   or when B is absent, X and A, together with the atoms to which         they are attached can form a heterocyclic ring, having from 5 to         8 ring atoms, wherein 1-2 ring atoms of the heterocyclic ring         system are selected from N, O and S;         B is a absent or

-   -   wherein R^(1b) and R^(2b), are independently selected from the         group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) substituted or unsubstituted C₂-C₆-alkenyl,         -   (d) substituted or unsubstituted C₂-C₆-alkynyl,         -   (e) substituted or unsubstituted aryl,         -   (f) substituted or unsubstituted heterocyclyl,         -   (g) substituted or unsubstituted heteroaryl,         -   (h) C₁-C₆-alkyl substituted with aryl,         -   (i) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (j) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1b) and R^(2b) together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S;     -   q is an integer of 0-4;         R₃ is H or substituted or unsubstituted C₁-C₆-alkyl,     -   or R₃ and A, together with the atoms to which they are attached         can form a substituted or unsubstituted 3-10 membered cycloalkyl         or a heterocyclic ring system, wherein the heterocyclic ring         system may have from 3 to 10 ring atoms, with 1 to 2 rings being         in the ring system and contain from 1-4 heteroatoms selected         from N, O and S;         R⁴ is H or substituted or unsubstituted C₁-C₆-alkyl,     -   or R⁴ and A, together with the atoms to which they are attached         can form a substituted or unsubstituted heterocyclic ring,         having from 3 to 8 ring atoms, wherein 1-2 ring atoms of the         heterocyclic ring system are selected from N, O and S;         n is an integer of 0-2;         A is selected from the group consisting of     -   (1) H,     -   (2) —(CH₂)_(r)C(R^(1a), R^(2a))(CH₂)_(s)OR^(3a),     -   (3) —(CH₂)_(r)C(R^(1a), R^(2a))N(R^(4a), R^(1a)),     -   (4) —(CH₂)_(r)C(R^(1a), R^(2a))N(R^(4a))COR^(3a),     -   (5) —(CH₂)_(r)C(R^(1a), R^(2a))NHCON(R^(4a), R^(5a)),     -   (6) —(CH₂)_(r)C(R^(1a), R^(2a))NHC(═NH)N(R^(4a), R^(5a)),     -   (7) —CH(R^(1a), R^(2a)),     -   (8) —C≡CH,     -   (9) —(CH₂)_(r)C(R^(1a), R^(2a))CN,     -   (10) —(CH₂)_(r)C(R^(1a), R^(2a))CO₂R^(3a), and     -   (11) —(CH₂)_(r)C(R^(1a), R^(2a))CN(R^(4a), R^(5a))     -   wherein R^(1a), R^(2a), R^(3a), R^(4a), and R^(5a) are         independently selected from the group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) substituted or unsubstituted aryl,         -   (d) substituted or unsubstituted heterocyclyl,         -   (e) substituted or unsubstituted heteroaryl,         -   (f) C₁-C₆-alkyl substituted with aryl,         -   (g) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (h) C₁-C₆-alkyl substituted with heteroaryl,         -   or R^(4a) and R^(5a) together with the N atom to which they             are attached can form a substituted or unsubstituted             heterocyclic ring, having from 3 to 8 ring atoms, wherein             1-2 ring atoms of the heterocyclic ring system are selected             from N, O and S;     -   r is an integer of 0-4;     -   s is an integer of 0-4;         Q is absent or selected from the group consisting of     -   (1) —C(═O)N(R₁, R₂),     -   (2) —NHC(═O)N(R₁, R₂),     -   (3) —N(OH)C(═O)N(R₁, R₂),     -   (4) —CH(OH)C(═O)N(R₁, R₂),     -   (5) —CH[N(R^(2q), R^(1q))]C(═O)N(R₁, R₂),     -   (6) —CHR^(1q)C(═O)N(R₁, R₂),     -   (7) —CO₂H,     -   (8) —C(═O)NHSO₂R^(4q),     -   (9) —SO₂NH₂,     -   (10) —N(OH)C(═O)R^(1q),     -   (11) —N(OH)SO₂R^(4q).     -   (12) —NHSO₂R^(4q),     -   (13) —SH,     -   (14) —CH(SH)(CH₂)₀₋₁C(═O)N(R₁, R₂),     -   (15) —CH(SH)(CH₂)₀₋₁CO₂H,     -   (16) —CH(OH)(CH₂)₀₋₁CO₂H,     -   (17) —CH(SH)CH₂CO₂R^(1q),     -   (18) —CH(OH)(CH₂)SO₂NH₂,     -   (19) —CH(CH₂SH)NHCOR^(1q),     -   (20) —CH(CH₂SH)NHSO₂R^(4q),     -   (21) —CH(CH₂SR^(5q))CO₂H,     -   (22) —CH(CH₂SH)NHSO₂NH₂,     -   (23) —CH(CH₂OH)CO₂H,     -   (24) —CH(CH₂OH)NHSO₂NH₂,     -   (25) —C(═O)CH₂CO₂H,     -   (26) —C(═O)(CH₂)₀₋₁CONH₂,     -   (27) —OSO₂NHR^(5q),     -   (28) —SO₂NHNH₂,     -   (29) —P(═O)(OH)₂,

-   -   (30)     -   (31)     -   (32)         R₁, is selected from the group consisting of     -   (1) —H,     -   (2) —OH,     -   (3) —OC₁₋₆-alkyl,     -   (4) —N(R^(2q), R^(3q)), and     -   (5) substituted or unsubstituted C₁₋₆-alkyl;         R₂ is selected from the group consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted C₂-C₆-alkenyl,     -   (4) substituted or unsubstituted C₂-C₆-alkenyl,     -   (5) substituted or unsubstituted aryl,     -   (6) substituted or unsubstituted heterocyclyl,     -   (7) substituted or unsubstituted heteroaryl,     -   (8) C₁-C₆-alkyl substituted with aryl,     -   (9) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (10) C₁-C₆-alkyl substituted with heteroaryl,     -   or R¹ and R², together with the N atom to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S,     -   R^(1q), R^(2q), R^(3q), R^(4q), and R^(5q) are selected from H         or C₁-C₆ alkyl,         wherein B is absent, or E, L, G, and B are absent, or E, L, and         G are absent, or E, L, and B are absent, or E, L, D, G, and B         are absent.         In another embodiment, the present invention provides compounds         of formula I:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl, and     -   (5) substituted or unsubstituted heteroaryl;         L is absent or selected from the group consisting of     -   (1) —(CH₂)_(j)—NR^(3L)—(CH₂)_(k)—,     -   (2) —C(R^(1L), R^(2L))_(j)—NR^(3L)—(R^(1L), R^(2L)),     -   (3) —C(R^(1L), R^(2L))_(j)—O—C(R^(1L), R^(2L))_(k)—,     -   (4) —(CH₂)_(j)—NR^(3L)—C(R^(1L), R^(2L))_(k)—CONH—(CH₂)_(k)—,     -   (5) —CO—C(R^(1L), R^(2L))—NHCO—,     -   (6) —CONH—, and     -   (7) —NHCO—,     -   wherein     -   R^(1L), R^(2L), R^(3L) are independently selected from the group         consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) C₁-C₆-alkyl substituted with aryl,         -   (d) C₁-C₆-alkyl substituted with heterocyclyl,         -   (e) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 5 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S;     -   j is an integer of 0-4;     -   k is an integer of 0-4;         D is absent or selected from the group consisting of     -   (1) substituted or unsubstituted C₃-C₈-cycloalkyl,     -   (2) substituted or unsubstituted aryl,     -   (3) substituted or unsubstituted heterocyclyl,     -   (4) substituted or unsubstituted heteroaryl, and         G is absent or selected from the group consisting of     -   (1) —C(═O)—,     -   (2) —NHC(═O)—,     -   (3) —C(═O)NH—,     -   (4) —(CH₂)_(i)NHCH₂C(═O)NH—,     -   (5) —C≡C—, and     -   (6) —C≡C—C≡C—,     -   wherein i is an interger of 0-4;         Y is selected from the group consisting of     -   (1) substituted or unsubstituted C₃-C₈-cycloalkyl,     -   (2) substituted or unsubstituted aryl,     -   (3) substituted or unsubstituted heterocyclyl, and     -   (4) substituted or unsubstituted heteroaryl;         X is selected from the group consisting of     -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-C═O)—,     -   (3) —C₂-C₆-alkenyl-(C═O),     -   (4) —C₂-C₆-alkynyl-(C═O)—, and     -   (5) —CH₂—;     -   or when B is absent, X and A, together with the atoms to which         they are attached can form a heterocyclic ring, having from 5 to         8 ring atoms, wherein 1-2 ring atoms of the heterocyclic ring         system are selected from N, O and S;         B is absent or

-   -   wherein R^(1b) and R^(2b) are independently selected from the         group consisting of         -   (a) H         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) substituted or unsubstituted C₂-C₆-alkenyl,         -   (d) substituted or unsubstituted C₂-C₆-alkenyl,         -   (e) substituted or unsubstituted aryl,         -   (f) substituted or unsubstituted heterocyclyl,         -   (g) substituted or unsubstituted heteroaryl,         -   (h) C₁-C₆-alkyl substituted with aryl,         -   (i) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (j) C₁-C₆-alkyl substituted with heteroaryl,         -   or R^(1b) and R^(2b), together with the atoms to which they             are attached can form a substituted or unsubstituted             heterocyclic ring, having from 5 to 8 ring atoms, wherein             1-2 ring atoms of the heterocyclic ring system are selected             from N, O and S;     -   q is an integer of 0-2;         R₃ is H or substituted or unsubstituted C₁-C₆-alkyl,     -   or R₃ and A, together with the atoms to which they are attached         can form a substituted or unsubstituted 3-10 membered cycloalkyl         or a heterocyclic ring system, wherein the heterocyclic ring         system may have from 3 to 10 ring atoms, with 1 to 2 rings being         in the ring system and contain from 1-4 heteroatoms selected         from N, O and S;         R⁴ is H or substituted or unsubstituted C₁-C₆-alkyl,     -   or R⁴ and A, together with the atoms to which they are attached         can form a substituted or unsubstituted heterocyclic ring,         having from 5 to 8 ring atoms, wherein 1-2 ring atoms of the         heterocyclic ring system are selected from N, O and S;         A is selected from the group consisting of     -   (1) H,     -   (2) —(CH₂)_(r)C(R^(1a), R^(2a))(CH₂) OR^(3a),     -   (3) —(CH₂)_(r)C(R^(1a), R^(2a))N(R^(4a), R^(5a)),     -   (4) —(CH₂)_(r)C(R^(1a), R^(2a))N(R^(4a))COR^(3a),     -   (5) —(CH₂)_(r)C(R^(1a), R^(2a))NHCON(R^(4a), R^(1a)),     -   (6) —(CH₂)_(r)C(R^(1a), R^(2a))NHC(═NH)N(R^(1a), R^(5a)),     -   (7) —CH(R^(1a), R^(2a)),     -   (8) —C≡CH,     -   (9) —(CH₂)_(r)C(R^(1a), R^(2a))CN, and     -   (10) —(CH₂)_(r)C(R^(1a), R^(2a))CO₂R^(3a),     -   wherein R^(1a), R^(2a), R^(3a), R^(4a), and R^(5a), are         independently selected from the group consisting of         -   (a) H,         -   (b) substituted or unsubstituted C₁-C₆-alkyl,         -   (c) C₁-C₆-alkyl substituted with aryl,         -   (d) C₁-C₆-alkyl substituted with heterocyclyl, and         -   (e) C₁-C₆-alkyl substituted with heteroaryl,         -   or R^(4a) and R^(5a), together with the N atom to which they             are attached can form a substituted or unsubstituted             heterocyclic ring, having from 5 to 8 ring atoms, wherein             1-2 ring atoms of the heterocyclic ring system are selected             from N, O and S;     -   r is an integer of 0-4;         Q is absent or selected from the group consisting of     -   (1) —C(═O)N(R₁, R₂),     -   (2) —NHC(═O)N(R₁, R₂),     -   (3) —N(OH)C(═O)N(R₁, R₂),     -   (4) —CH(OH)C(═O)N(R₁, R₂),     -   (5) —CH[N(R^(2q), R^(1q))]C(═O)N(R₁, R₂), and     -   (6) —CHR^(1q)C(═O)N(R₁, R₂),         R₁ is selected from the group consisting of     -   (1) H,     -   (2) OH,     -   (3) OC₁₋₆-alkyl,     -   (4) N(R^(2q), R^(3q)), and     -   (5) substituted or unsubstituted C₁₋₆-alkyl;         R₂ is selected from the group consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl,     -   (5) substituted or unsubstituted heteroaryl,     -   (6) C₁-C₆-alkyl substituted with aryl,     -   (7) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (8) C₁-C₆-alkyl substituted with heteroaryl,     -   or R¹ and R², together with the N atom to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S,     -   R^(1q), R^(2a), and R^(3q) are selected from H or C₁-C₆ alkyl,         wherein B is absent, or E, L, G, and B are absent, or E, L, and         G are absent, or E, L, and B are absent, or E, L, D, G, and B         are absent.         In another embodiment, the present invention provides compounds         of formula II:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

X is selected from the group consisting of

-   -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-(C═O)—, and     -   (3) —C₂-C₆-alkenyl-(C═O)—.         In another embodiment, the present invention provides compounds         of formula III:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

X is selected from the groups consisting of

-   -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-(C═O)—, and     -   (3) —C₂-C₆-alkenyl-(C═O)—.         In another embodiment, the present invention provides compounds         of formula IV:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

X is selected from the groups consisting of

-   -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-(C═O)—, and     -   (3) —C₂-C₆-alkenyl-(C═O)—.         In another embodiment, the present invention provides compounds         of formula V:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

X is selected from the groups consisting of

-   -   (1) —(C═O)—,     -   (2) —C₁-C₆-alkyl-(C═O)—, and     -   (3) —C₂-C₆-alkenyl-(C═O)—.         In another embodiment, the present invention provides compounds         of formula VI:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl, and     -   (5) substituted or unsubstituted heteroaryl,     -   or E and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S,         R^(1L), R^(3L) are independently selected from the group         consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S.         In another embodiment, the present invention provides compounds         of formula VII:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl, and     -   (5) substituted or unsubstituted heteroaryl,     -   or E and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S;         R^(1L), R^(3L) are independently selected from the group         consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S.         In another embodiment, the present invention provides compounds         of formula VIII:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl, and     -   (5) substituted or unsubstituted heteroaryl,     -   or E and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S;         R^(1L), R^(3L) are independently selected from the group         consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S.         In another embodiment, the present invention provides compounds         of formula IX:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl, and     -   (5) substituted or unsubstituted heteroaryl,     -   or E and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S;         R^(1L), R^(3L) are independently selected from the group         consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S.         In another embodiment, the present invention provides compounds         of formula X:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is absent or selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl, and     -   (5) substituted or unsubstituted heteroaryl,     -   or E and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 10 ring atoms, wherein 1-4 ring atoms of         the heterocyclic ring system are selected from N, O and S;         R^(1L), R^(3L) are independently selected from the group         consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl,     -   or R^(1L) and R^(3L), together with the atoms to which they are         attached can form a substituted or unsubstituted heterocyclic         ring, having from 3 to 8 ring atoms, wherein 1-2 ring atoms of         the heterocyclic ring system are selected from N, O and S.         In another embodiment, the present invention provides compounds         of formula XI:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein Y—X taken together, is selected from the group consisting of

In another embodiment, the present invention provides compounds of formula XII:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein R^(1b) and R^(2b) are independently selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted C₂-C₆-alkenyl,     -   (4) substituted or unsubstituted C₂-C₆-alkenyl,     -   (5) substituted or unsubstituted aryl,     -   (6) substituted or unsubstituted heterocyclyl,     -   (7) substituted or unsubstituted heteroaryl,     -   (8) C₁-C₆-alkyl substituted with aryl,     -   (9) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (10) C₁-C₆-alkyl substituted with heteroaryl;         q is an integer of 0-2;         In another embodiment, the present invention provides compounds         of formula XIII:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein R⁴ is selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl;         A is H or —CH(CH₃)OH—;         R₁ is H or substituted or unsubstituted C₁₋₆-alkyl;         R₂ is selected from the group consisting of     -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) substituted or unsubstituted aryl,     -   (4) substituted or unsubstituted heterocyclyl,     -   (5) substituted or unsubstituted heteroaryl,     -   (6) C₁-C₆-alkyl substituted with aryl,     -   (7) C₁-C₆-alkyl substituted with heterocyclyl,     -   (8) C₁-C₆-alkyl substituted with heteroaryl,     -   or R¹ and R² together with the N atom to which they are attached         can form a substituted or unsubstituted heterocyclic ring,         having from 3 to 10 ring atoms, wherein 1-2 ring atoms of the         heterocyclic ring system are selected from N, O and S.         In another embodiment, the present invention provides compounds         of formula XIV:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

R⁴ is selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl.         In another embodiment, the present invention provides compounds         of formula XV:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

In another embodiment, the present invention provides compounds of formula XVI:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

R⁴ is selected from the group consisting of

-   -   (1) H,     -   (2) substituted or unsubstituted C₁-C₆-alkyl,     -   (3) C₁-C₆-alkyl substituted with aryl,     -   (4) C₁-C₆-alkyl substituted with heterocyclyl, and     -   (5) C₁-C₆-alkyl substituted with heteroaryl;         In another embodiment, the present invention provides compounds         of formula XVII:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein D-G-Y taken together, is selected from the group consisting of

Wherein

R is selected from the group consisting of —CH₃, —C₂H₅, —CH₂OH, —OH, —OCH₃, —OC₂H₅, —OCF₃, —CN, —NO₂, —CO₂H, —CO₂CH₃, —CONH₂, —NH₂, —F, —Cl, —Br, —CF₃, —N(CH₃)₂, —NHSO₂CH₃, and —NHCOCH₃;

In one aspect, the invention provides a method of inhibiting a deacetylase enzyme in a gram-negative bacteria, thereby affecting bacterial growth, comprising administering to a patient in need of such inhibition a compound of formula I.

In another aspect, the invention provides a method of inhibiting LpxC, thereby modulating the virulence of a bacterial infection, comprising administering to a patient in need of such inhibition a compound of formula I.

In some embodiments of the method of inhibiting LpxC using a compound of formula I, the IC₅₀ value of the compound is less than or equal to 10 μM with respect to LpxC. In other such embodiments, the IC₅₀ value is less than or equal to 1 μM, is less than or equal to 0.1 μM, is less than or equal to 0.050 μM, is less than or equal to 0.030 μM, is less than or equal to 0.025 μM, or is less than or equal to 0.010 μM.

In one aspect of the invention, methods for treating a subject comprising administering to the subject an antibacterially effective amount of a compound of formula I, together with a pharmaceutically acceptable carrier is provided. In a preferred embodiment of the method of treatment, the subject is a mammal and some embodiments, a human.

In another aspect, the invention provides a method of administering an inhibitory amount of a compound of formula I to fermentative or non-fermentative gram-negative bacteria. In a preferred embodiment of the method of administering an inhibitory amount of a compound of formula I to fermentative or non-fermentative gram-negative bacteria, the gram-negative bacteria are selected from the group consisting of Pseudomonas aeruginosa, Stenotrophomonas maltophila, Burkholderia cepacia, Alcaligenes xylosoxidans, Acinetobacter, Enterobacteriaceae, Haemophilus, Neisseria species.

In another embodiment, the invention provides a method of administering an inhibitory amount of a compound of formula I to gram-negative bacteria, such as Enterobacteriaceae that is selected from the group consisting of organisms such as Serratia, Proteus, Klebsiella, Enterobacter, Citrobacter, Salmonella, Providencia, Morganella, Cedecea, and Edwardsiella species and Escherichia coli.

Another embodiment of the invention provides a pharmaceutical composition comprising an effective amount of a compound of Formula I with a pharmaceutically acceptable carrier thereof.

Pharmaceutical formulations according to the present invention are provided which include any of the compounds described above in combination with a pharmaceutically acceptable carrier.

Another embodiment of the invention provides a method of co-administering the compound of formula I with other therapeutic agents that are selected for their particular usefulness against the condition that is being treated.

For example, the compound of formula I is useful in combination with other anti-bacterial agents. The compound of formula I augments the sensitivity of gram-negative bacteria to existing classes of antibacterials. Combinations of the presently disclosed compounds with other anti-bacterial agents are within the scope of the invention. Such anti-bacterial agents include, but are not limited to, erythromycin, rifampicin, Nalidixic acid, carbenicillin, bacitracin, cycloserine, fosfomycin, and vancomycin.

A further aspect of the invention is the use of LpxC inhibitors for the treatment of an infection, particularly a bacterial infection. A bacterial infection treated with the compounds of the invention can be a primary infection or a co-infection caused by a species of bacteria and one or more additional infectious agents selected from the group consisting of bacteria, virus, parasite and fungus.

The term “treating”, as used herein, refers to reversing, alleviating, inhibiting the progress of, or preventing the disorder or condition to which such term applies, or one or more symptoms of such disorder or condition. The term “treatment”, as used herein, refers to the act of treating, as “treating” is defined immediately above.

The compounds of the invention can be used for treating conditions caused by the bacterial production of endotoxin and, in particular, by gram-negative bacteria and bacteria that use LpxC in the biosynthesis of lipopolysaccharide (LPS) or endotoxin.

The compounds of the invention also are useful in the conditions that are caused or exacerbated by the bacterial production of lipid A and LPS or endotoxin, such as sepsis, septic shock, systemic inflammation, localized inflammation, chronic obstructive pulmonary disease (COPD) and acute exacerbations of chronic bronchitis (AECB). For these conditions, treatment includes the administration of a compound of the invention, or a combination of compounds of the invention, optionally with a second agent wherein the second agent is a second antibacterial agent or a second non-antibacterial agent.

For sepsis, septic shock, systemic inflammation, localized inflammation, chronic obstructive pulmonary disease (COPD) and acute exacerbations of chronic bronchitis (AECB), preferred second non-antibacterial agents include antiendotoxins including endotoxin receptor-binding antibodies, endotoxin-binding antibodies, antiCD14-binding protein antibodies antilipopolysaccharide-binding protein antibodies and tyrosine kinase inhibitors.

In treatment of serious or chronic respiratory tract infections, the compounds of the present invention may also be used with second non-antibacterial agents administered via inhalation. Preferred non-antibacterial agents used in this treatment include anti-inflammatory steroids, non-steroidal anti-inflammatory agents, bronchiodilators, mucolytics, anti-asthma therapeutics and lung fluid surfactants. In particular, the non-antibacterial agent may be selected from a group consisting of albuterol, salbuterol, budesonide, beclomethasone, dexamethasone, nedocromil, beclomethasone, fluticasone, flunisolide, triamcinolone, ibuprofin, rofecoxib, naproxen, celecoxib, nedocromil, ipratropium, metaproterenol, pirbuterol, salmeterol, bronchiodilators, mucolytics, calfactant, beractant, poractant alfa, surfaxin and pulmozyme (also called dornase alfa).

The compounds of the invention can be used, alone or in combination with a second antibacterial agent for the treatment of a serious or chronic respiratory tract infection including serious lung and nosocomial infections such as those caused by Enterobacter aerogenes, Enterobacter cloacae, Escherichia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Proteus mirabilis, Serratia marcescens, Stenotrophomonas maltophilia, Pseudomonas aeruginosa, Burkholderia cepacia, Acinetobacter calcoaceticus, Alcaligenes xylosoxidans, Flavobacterium meningosepticum, Providencia stuartii and Citrobacter freundi, community lung infections such as those caused by Haemophilus Influenzae, Legionella species, Moraxella catarrhalis, Branhamella catarrhalis, Enterobacter species, Acinetobacter species, Klebsiella species, and Proteus species, and infections caused by other bacterial species such as Neisseria species, Shigella species, Salmonella species, Helicobacter pylori, Vibrionaceae and Bordetella species as well as the infections is caused by a Brucella species, Francisella tularensis and/or Yersinia Pestis.

When used for treating Gram-negative bacteria, the compounds of the present invention can be used to sensitize gram-negative bacteria to the effects of a second agent.

When the compounds of the present invention are used in combination with a second antibacterial agent, non-limiting examples of antibacterial agents may be selected from the following groups:

-   -   (1) Macrolides or ketolides such as erythromycin, azithromycin,         clarithromycin and telithromycin;     -   (2) Beta-lactams including penicillin, cephalosporin, and         carbapenems such as carbapenem, imipenem, and meropenem;     -   (3) Monobactams such as penicillin G, penicillin V, methicillin,         oxacillin, cloxacillin, dicloxacillin, nafcillin, ampicillin,         amoxicillin, carbenicillin, ticarcillin, mezlocillin,         piperacillin, azlocillin, temocillin, cepalothin, cephapirin,         cephradine, cephaloridine, cefazolin, cefamandole, cefuroxime,         cephalexin, cefprozil, cefaclor, loracarbef, cefoxitin,         cefmetazole, cefotaxime, ceftizoxime, ceftriaxone, cefoperazone,         ceftazidime, cefixime, cefpodoxime, ceftibuten, cefdinir,         cefpirome, cefepime, and astreonam;     -   (4) Quinolones such as nalidixic acid, oxolinic acid,         norfloxacin, pefloxacin, enoxacin, ofloxacin, levofloxacin,         ciprofloxacin, temafloxacin, lomefloxacin, fleroxacin,         grepafloxacin, sparfloxacin, trovafloxacin, clinafloxacin,         gatifloxacin, moxifloxacin, sitafloxacin, ganefloxacin,         gemifloxacin and pazufloxacin;     -   (5) Antibacterial sulfonamides and antibacterial         sulphanilamides, including para-aminobenzoic acid, sulfadiazine,         sulfisoxazole, sulfamethoxazole and sulfathalidine;     -   (6) Aminoglycosides such as streptomycin, neomycin, kanamycin,         paromycin, gentamicin, tobramycin, amikacin, netilmicin,         spectinomycin, sisomicin, dibekalin and isepamicin;     -   (7) Tetracyclines such as tetracycline, chlortetracycline,         demeclocycline, minocycline, oxytetracycline, methacycline,         doxycycline;     -   (8) Rifamycins such as rifampicin (also called rifampin),         rifapentine, rifabutin, bezoxazinorifamycin and rifaximin;     -   (9) Lincosamides such as lincomycin and clindamycin;     -   (10) Glycopeptides such as vancomycin and teicoplanin;     -   (11) Streptogramins such as quinupristin and daflopristin;     -   (12) Oxazolidinones such as linezolid;     -   (13) Polymyxin, colistin and colymycin;     -   (14) Trimethoprim and bacitracin.

The second antibacterial agent may be administered in combination with the compounds of the present inventions wherein the second antibacterial agent is administered prior to, simultaneously, or after the compound or compounds of the present invention. When simultaneous administration of a compound of the invention with a second agent is desired and the route of administration is the same, then a compound of the invention may be formulated with a second agent into the same dosage form. An example of a dosage form containing a compound of the invention and a second agent is a tablet or a capsule.

When used for treating a serious or chronic respiratory tract infections, the compounds of the invention may be used alone or in combination with a second antibacterial agent administered via inhalation. In the case of inhalation, a preferred second antibacterial agent is selected from a group consisting of tobramycin, gentamicin, aztreonam, ciprofloxacin, polymyxin, colistin, colymycin, azithromycin and clarithromycin.

Pharmaceutical Compositions

Pharmaceutical compositions of the present invention comprise a therapeutically effective amount of a compound of the present invention formulated together with one or more pharmaceutically acceptable carriers. As used herein, the term “pharmaceutically acceptable carrier” means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials that can serve as pharmaceutically acceptable carriers are sugars such as lactose, glucose and sucrose; starches such as corn starch and potato starch; cellulose and its derivatives such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as cocoa butter and suppository waxes; oils such as peanut oil, cottonseed oil; safflower oil; sesame oil; olive oil; corn oil and soybean oil; glycols; such a propylene glycol; esters such as ethyl oleate and ethyl laurate; agar; buffering agents such as magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator. The pharmaceutical compositions of this invention can be administered to humans and other animals orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments, or drops), bucally, or as an oral or nasal spray, or a liquid aerosol or dry powder formulation for inhalation.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethylformamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor, and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof. Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.

Injectable preparations, for example, sterile injectable aqueous or oleaginous suspensions may be formulated according to the known art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution, suspension or emulsion in a nontoxic parenterally acceptable diluent or solvent, for example, as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, U.S.P. and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil can be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid are used in the preparation of injectables.

The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions that can be dissolved or dispersed in sterile water or other sterile injectable medium prior to use.

In order to prolong the effect of a drug, it is often desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution that, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form may be accomplished by dissolving or suspending the drug in an oil vehicle. Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations may also be prepared by entrapping the drug in liposomes or microemulsions that are compatible with body tissues.

Compositions for rectal or vaginal administration are preferably suppositories that can be prepared by mixing the compounds of this invention with suitable non-irritating excipients or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at ambient temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.

Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such solid dosage forms, the active compound is mixed with at least one inert, pharmaceutically acceptable excipient or carrier such as sodium citrate or dicalcium phosphate and/or a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol, and silicic acid, b) binders such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidinone, sucrose, and acacia, c) humectants such as glycerol, d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents such as paraffin, f) absorption accelerators such as quaternary ammonium compounds, g) wetting agents such as, for example, acetyl alcohol and glycerol monostearate, h) absorbents such as kaolin and bentonite clay, and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.

The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings and other coatings well known in the pharmaceutical formulating art. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.

The active compounds can also be in micro-encapsulated form with one or more excipients as noted above. The solid dosage forms of tablets, dragees, capsules, pills, and granules can be prepared with coatings and shells such as enteric coatings, release controlling coatings and other coatings well known in the pharmaceutical formulating art. In such solid dosage forms the active compound may be admixed with at least one inert diluent such as sucrose, lactose or starch. Such dosage forms may also comprise, as is normal practice, additional substances other than inert diluents, e.g., tableting lubricants and other tableting aids such a magnesium stearate and microcrystalline cellulose. In the case of capsules, tablets and pills, the dosage forms may also comprise buffering agents. They may optionally contain opacifying agents and can also be of a composition that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes.

Dosage forms for topical or transdermal administration of a compound of this invention include ointments, pastes, creams, lotions, gels, powders, solutions, sprays, inhalants or patches. The active component is admixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives or buffers as may be required. Ophthalmic formulations, ear drops, and the like are also contemplated as being within the scope of this invention.

The ointments, pastes, creams and gels may contain, in addition to an active compound of this invention, excipients such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Compositions of the invention may also be formulated for delivery as a liquid aerosol or inhalable dry powder. Liquid aerosol formulations may be nebulized predominantly into particle sizes that can be delivered to the terminal and respiratory bronchioles where bacteria reside in patients with bronchial infections, such as chronic bronchitis and pneumonia. Pathogenic bacteria are commonly present throughout airways down to bronchi, bronchioli and lung parenchema, particularly in terminal and respiratory bronchioles. During exacerbation of infection, bacteria can also be present in alveoli. Liquid aerosol and inhalable dry powder formulations are preferably delivered throughout the endobronchial tree to the terminal bronchioles and eventually to the parenchymal tissue.

Aerosolized formulations of the invention may be delivered using an aerosol forming device, such as a jet, vibrating porous plate or ultrasonic nebulizer, preferably selected to allow the formation of a aerosol particles having with a mass medium average diameter predominantly between 1 to 5 μm. Further, the formulation preferably has balanced osmolarity ionic strength and chloride concentration, and the smallest aerosolizable volume able to deliver effective dose of the compounds of the invention to the site of the infection. Additionally, the aerosolized formulation preferably does not impair negatively the functionality of the airways and does not cause undesirable side effects.

Aerosolization devices suitable for administration of aerosol formulations of the invention include, for example, jet, vibrating porous plate, ultrasonic nebulizers and energized dry powder inhalers, that are able to nebulize the formulation of the invention into aerosol particle size predominantly in the size range from 1-5 μm. Predominantly in this application means that at least 70% but preferably more than 90% of all generated aerosol particles are 1 to 5 μm range. A jet nebulizer works by air pressure to break a liquid solution into aerosol droplets. Vibrating porous plate nebulizers work by using a sonic vacuum produced by a rapidly vibrating porous plate to extrude a solvent droplet through a porous plate. An ultrasonic nebulizer works by a piezoelectric crystal that shears a liquid into small aerosol droplets. A variety of suitable devices are available, including, for example, AeroNeb and AeroDose vibrating porous plate nebulizers (AeroGen, Inc., Sunnyvale, Calif.), Sidestream7 nebulizers (Medic-Aid Ltd., West Sussex, England), Pari LC7 and Pari LC Star7 jet nebulizers (Pari Respiratory Equipment, Inc., Richmond, Va.), and Aerosonic (DeVilbiss Medizinische Produkte (Deutschland) GmbH, Heiden, Germany) and UltraAire7 (Omron Healthcare, Inc., Vernon Hills, Ill.) ultrasonic nebulizers.

Compounds of the invention may also be formulated for use as topical powders and sprays that can contain, in addition to the compounds of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants such as chlorofluorohydrocarbons.

Transdermal patches have the added advantage of providing controlled delivery of a compound to the body. Such dosage forms can be made by dissolving or dispensing the compound in the proper medium. Absorption enhancers can also be used to increase the flux of the compound across the skin. The rate can be controlled by either providing a rate controlling membrane or by dispersing the compound in a polymer matrix or gel.

According to the methods of treatment of the present invention, bacterial infections are treated or prevented in a patient such as a human or lower mammal by administering to the patient a therapeutically effective amount of a compound of the invention, in such amounts and for such time as is necessary to achieve the desired result. By a “therapeutically effective amount” of a compound of the invention is meant a sufficient amount of the compound to treat bacterial infections, at a reasonable benefit/risk ratio applicable to any medical treatment. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; the activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well known in the medical arts.

The total daily dose of the compounds of this invention administered to a human or other mammal in single or in divided doses can be in amounts, for example, from 0.01 to 50 mg/kg body weight or more usually from 0.1 to 25 mg/kg body weight. Single dose compositions may contain such amounts or submultiples thereof to make up the daily dose. In general, treatment regimens according to the present invention comprise administration to a patient in need of such treatment from about 10 mg to about 2000 mg of the compound(s) of this invention per day in single or multiple doses.

Methods of formulation are well known in the art and are disclosed, for example, in Remington: The Science and Practice of Pharmacy, Mack Publishing Company, Easton, Pa., 19th Edition (1995). Pharmaceutical compositions for use in the present invention can be in the form of sterile, non-pyrogenic liquid solutions or suspensions, coated capsules, suppositories, lyophilized powders, transdermal patches or other forms known in the art.

A “kit” as used in the instant application includes a container for containing the pharmaceutical compositions and may also include divided containers such as a divided bottle or a divided foil packet. The container can be in any conventional shape or form as known in the art that is made of a pharmaceutically acceptable material, for example a paper or cardboard box, a glass or plastic bottle or jar, a resealable bag (for example, to hold a “refill” of tablets for placement into a different container), or a blister pack with individual doses for pressing out of the pack according to a therapeutic schedule. The container employed can depend on the exact dosage form involved, for example a conventional cardboard box would not generally be used to hold a liquid suspension. It is feasible that more than one container can be used together in a single package to market a single dosage form. For example, tablets may be contained in a bottle that is in turn contained within a box.

An example of such a kit is a so-called blister pack. Blister packs are well known in the packaging industry and are being widely used for the packaging of pharmaceutical unit dosage forms (tablets, capsules, and the like). Blister packs generally consist of a sheet of relatively stiff material covered with a foil of a preferably transparent plastic material. During the packaging process, recesses are formed in the plastic foil. The recesses have the size and shape of individual tablets or capsules to be packed or may have the size and shape to accommodate multiple tablets and/or capsules to be packed. Next, the tablets or capsules are placed in the recesses accordingly and the sheet of relatively stiff material is sealed against the plastic foil at the face of the foil that is opposite from the direction in which the recesses were formed. As a result, the tablets or capsules are individually sealed or collectively sealed, as desired, in the recesses between the plastic foil and the sheet. Preferably the strength of the sheet is such that the tablets or capsules can be removed from the blister pack by manually applying pressure on the recesses whereby an opening is formed in the sheet at the place of the recess. The tablet or capsule can then be removed via said opening.

It maybe desirable to provide a written memory aid, where the written memory aid is of the type containing information and/or instructions for the physician, pharmacist or other health care provider, or subject, e.g., in the form of numbers next to the tablets or capsules whereby the numbers correspond with the days of the regimen that the tablets or capsules so specified should be ingested or a card that contains the same type of information. Another example of such a memory aid is a calendar printed on the card e.g., as follows “First Week, Monday, Tuesday,” . . . etc. . . . “Second Week, Monday, Tuesday, . . . ” etc. Other variations of memory aids will be readily apparent. A “daily dose” can be a single tablet or capsule or several tablets or capsules to be taken on a given day. When the kit contains separate compositions, a daily dose of one or more compositions of the kit can consist of one tablet or capsule while a daily dose of another one or more compositions of the kit can consist of several tablets or capsules.

Another specific embodiment of a kit is a dispenser designed to dispense the daily doses one at a time in the order of their intended use. Preferably, the dispenser is equipped with a memory-aid, so as to further facilitate compliance with the regimen. An example of such a memory-aid is a mechanical counter, that indicates the number of daily doses that has been dispensed. Another example of such a memory-aid is a battery-powered micro-chip memory coupled with a liquid crystal readout, or audible reminder signal that, for example, reads out the date that the last daily dose has been taken and/or reminds one when the next dose is to be taken.

The kits of the present invention may also include, in addition to LpxC inhibitors, one or more additional pharmaceutically active compounds. Preferably, the additional compound is another LpxC inhibitor or another compound useful to bacterial infections. The additional compounds may be administered in the same dosage form as the LpxC inhibitor or in different dosage forms. Likewise, the additional compounds can be administered at the same time as the LpxC inhibitor or at different times.

Compositions of the present compounds may also be used in combination with other known antibacterial agents of similar spectrum to (1) synergistically enhance treatment of severe Gram-negative infections covered by the spectrum of this compound or (2) add coverage in severe infections in which multiple organisms are suspected in which another agent of a different spectrum may be required in addition to this compound. Potential agents include members of the aminoglycosides, penicillins, cephalosporins, fluoroquinolones, macrolides, glycopeptides, lipopeptides and oxazolidinones. The treatment can involve administering a composition having both active agents or administration of the inventive compounds followed by or preceded by administration of an additional active antibacterial agent.

Characterization and Purification Methods

Referring to the examples that follow, compounds of the present invention were characterized by high performance liquid chromatography (HPLC) using a Waters Millenium chromatography system with a 2690 Separation Module (Milford, Mass.). The analytical columns were Alltima C-18 reversed phase, 4.6×250 mm from Alltech (Deerfield, Ill.). A gradient elution was used, typically starting with 5% acetonitrile/95% water and progressing to 100% acetonitrile over a period of 40 minutes. All solvents contained 0.1% trifluoroacetic acid (TFA). Compounds were detected by ultraviolet light (UV) absorption at either 220 or 254 nm. HPLC solvents were from Burdick and Jackson (Muskegan, Mich.), or Fisher Scientific (Pittsburgh, Pa.). In some instances, purity was assessed by thin layer chromatography (TLC) using glass or plastic backed silica gel plates, such as, for example, Baker-Flex Silica Gel 1B2-F flexible sheets. TLC results were readily detected visually under ultraviolet light, or by employing well known iodine vapor and other various staining techniques.

Mass spectrometric analysis was performed on one of two LCMS instruments: a Waters System (Alliance HT HPLC and a Micromass ZQ mass spectrometer; Column: Eclipse XDB-C18, 2.1×50 mm; solvent system: 5-95% (or 35-95%, or 65-95% or 95-95%) acetonitrile in water with 0.05% TFA; flow rate 0.8 mL/min; molecular weight range 500-1500; cone Voltage 20 V; column temperature 40° C.) or a Hewlett Packard System (Series 1100 HPLC; Column: Eclipse XDB-C18, 2.1×50 mm; solvent system: 1-95% acetonitrile in water with 0.05% TFA; flow rate 0.4 mL/min; molecular weight range 150-850; cone Voltage 50 V; column temperature 30° C.). All masses are reported as those of the protonated parent ions.

GCMS analysis was performed on a Hewlet Packard instrument (HP6890 Series gas chromatograph with a Mass Selective Detector 5973; injector volume: 1 μL; initial column temperature: 50° C.; final column temperature: 250 C; ramp time: 20 minutes; gas flow rate: 1 mL/min; column: 5% phenyl methyl siloxane, Model #HP 190915-443, dimensions: 30.0 m×25 m×0.25 m).

Nuclear magnetic resonance (NMR) analysis was performed with a Varian 300 Mhz NMR (Palo Alto, Calif.). The spectral reference was either TMS or the known chemical shift of the solvent. Some compound samples were run at elevated temperatures (e.g. 75° C.) to promote increased sample solubility.

The purity of some of the invention compounds was assessed by elemental analysis (Desert Analytics, Tuscon, Ariz.)

Melting points were determined on a Laboratory Devices MeI-Temp apparatus (Holliston, Mass.).

Preparative separations were carried out using a Flash 40 chromatography system and KP-Sil, 60A (Biotage, Charlottesville, Va.), or by flash column chromatography using silica gel (230-400 mesh) packing material, or by HPLC using a C-18 reversed phase column. Typical solvents employed for the Flash 40 Biotage system and flash column chromatography were dichloromethane, methanol, ethyl acetate, hexane, acetone, aqueous hydroxyamine and triethyl amine. Typical solvents employed for the reverse phase HPLC were varying concentrations of acetonitrile and water with 0.1% trifluoroacetic acid.

Compounds of the present invention can be readily synthesized using the methods described herein, or other methods, that are well known in the art. For example, the synthesis of hydroxamic acids or similar scaffolds having a wide variety of substituents are comprehensively reviewed in Kline T, Andersen N H, Harwood E A, Bowman J, Malanda A, Endsley S, Erwin A L, Doyle M, Fong S, Harris A L, Mendelsohn B, Mdluli K, Raetz C R, Stover C K, Witte P R, Yabannavar A, Zhu S., “Potent, novel in vitro inhibitors of the Pseudomonas aeruginosa deacetylase LpxC,” J Med Chem 2002 Jul. 4; 45(14):3112-29; Patchett, A. A., Nargund, R., Chen, M.-H., Nishi, H. R., U.S. Pat. No. 5,925,659, 1999; Pirrung, M. C., Chau, J. H., “A Convenient Procedure for the Preparation of Amino Acid Hydroxamates from Esters,” J. Org. Chem. 1995, 60, 8084-8085; Nhu, K., Patel, D. V., “A New and Efficient Solid Phase Synthesis of Hydroxamic Acids,” J. Org. Chem. 1997, 62, 7088-7089; Patel, D., Nhu, K., “Methods for Solid-phase Synthesis of Hydroxylamine Compounds and Derivatives, and Combinatorial Libraries Thereof,” PCT WO 98/18754, 1998, Mellor, S. L., McGuire, C., Chan, W. C., “N-Fmoc-aminoxy-2-chlortrityl Polystyrene Resin: A Facile Solid-phase Methodology for the Synthesis of Hydroxamic Acids,” Tetrahedron Lett., 1997, 38, 3311-3314; Khan, S. I., Grinstaff, M. W., “A Facile and Convenient Solid-phase Procedure for Synthesizing Nucleoside Hydroxamic Acids,” Terahedron. Lett., 1998, 39, 8031-8034; Zhang, Y., Li, D., Houtman, J. C., Witiak, D. T., Seltzer, J., Bertics, P. J., Lauhon, C. T., “Design, Combinatorial Chemical Synthesis, and in vitro Characterization of Novel Urea Based Gelatinase Inhibitors,” Bioorg. Med. Chem. Lett., 1999, 9, 2823-2826; Ito, Y., Inubushi, Y., Zenbayashi, M., Tomita, S., Saegusa, T., “Synthetic Reactions by Complex Catalysts. XXXI, A Novel and Versatile Method of Heterocycle Synthesis,” J. Am Chem. Soc., 1973, 95, 4447-4448; Ito, Y., Ito, I., Hirao, T., Saegus, T., “Synthetic Reactions by Complex Catalysts XXXV,” Syn. Commun. 1974, 4, 97-103; Witte, H., Seliger, W., “Cyclische Imidsaurester aus Nitrilen und Aminoalkoholen,” Liebigs Ann. Chem., 1974, 996-1009; Pattenden, G., Thom. S. M., “Naturally Occurring Linear Fused Thiazoline-Thiazole Containing Metabolites: Total Synthesis of (−) Didehydromirabazole A, a Cytotoxic Alkaloid from Blue-Green Algae,” J. Chem. Soc. Perkin Trans 1, 1993, 1629-1636; Boyce, R. J., Mulqueen, G. C., Pattenden, G., “Total Synthesis of Thiangazole, A Novel Naturally Occurring HIV-1 Inhibitor from Polyangium sp.” Tetrahedron, 1995, 51, 7321-7330; Galeotti, N., Plagnes, E., Jouin, P., “Synthesis of Peptidyl Aldehydes from Thiazolines,” Tetrahedron. Lett. 1997, 38, 2459-2462; Charette, A. B., Chua, P., “Mild Method for the Synthesis of Thiazolines from Secondary and Tertiary Amides,” J. Org. Chem., 1998, 63, 908-909; Bergeron, R. J., Wiegand, J., McManis, J. S., McCosar, B. H., Weimar, W. R., Brittenham, G. M., Smith, R. E., “Effects of C-4 Stereochemistry and C-4′ Hydroxylation on the Iron Clearing Efficiency and Toxicity of Desferrithiocin Analogues,” J. Med. Chem. 1999, 42, 2432-2440; Raman, P., Razavik H., Kelly, J. W., “Titanium (IV)-mediated Tandem Deprotection-cyclodehydration of Protected Cysteine N-Amides: Biomimetic Synthesis of Thiazoline- and Thiazole-containing Heterocycles,” Org. Lett., 2000, 2, 3289-3292; Fernandez, X., Fellous, R., Dunach, E., “Novel Synthesis of 2-Thioazolines,” Tetrahedron Lett., 2000, 41, 3381-3384. Wipf, P., Miller, C. P., Venkatraman, S., Fritch, P., “C. Thiolysis of Oxazolinenes: A New, Selective Method for the Direct Conversion of Peptide Oxazolines into Thiazolines,” Tetrahedron Lett., 1995, 36, 6395-6398, which are incorporated herein by reference.

The synthesis of other non-hydroxamates compounds or more generally zinc binding groups are reviewed in Pirrung, M. C., Tumey, L. N., Raetz, C. R. H., Jackman, J. E., Snehalatha, K., McClerren, A. L., Fierke, C. A., Gantt, S. L., Rusche, K. M., “Inhibition of the Antibacterial Target UDP-(3-O-acyl)-N-acetylglucosamine Deacetylase (LpxC): Isoxazoline Zinc Amidase Inhibitors Bearing Diverse Metal Binding Groups,” Journal of Medicinal Chemistry (2002), 45(19), 4359-4370; Jackman, J. E., Fierke, C. A., Tumey, L. N., Pirrung, M., Uchiyama, T., Tahir, S. H., Hindsgaul, O., Raetz, C. R. H., “Antibacterial agents that target lipid A biosynthesis in gram-negative bacteria: inhibition of diverse UDP-3-O—(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylases by substrate analogs containing zinc binding motifs,” Journal of Biological Chemistry (2000), 275(15), 11002-11009; Brooks, C. D. W., Summers, J. B., “Modulators of Leukotriene Biosynthesis and Receptor Activation,” Journal of Medicinal Chemistry (1996), 39(14), 2629-2654; Jeng, A. Y., De Lombaert, S., “Endothelin converting enzyme inhibitors,” Current Pharmaceutical Design (1997), 3(6), 597-614; Zask, A., Levin, J. I., Killar, L. M., Skotnicki, J. S., “Inhibition of matrix metalloproteinases: structure based design,” Current Pharmaceutical Design (1996), 2(6), 624-661; Skotnicki, J. S., DiGrandi, M. J., Levin, J. I., Chemical and Screening Sciences, Wyeth Research, New York, N.Y., USA. Current Opinion in Drug Discovery & Development (2003), 6(5), 742-759.

The foregoing may be better understood by reference to the following examples, that are presented for illustration and not to limit the scope of the inventive concepts.

EXAMPLES

The following are abbreviations used in the examples:

-   -   AcOH: Acetic acid     -   aq: Aqueous     -   ATP: Adenosine triphosphate     -   Boc: tert-butoxycarbonyl     -   Boc-Thr(OBn)-OH         3-(R)-Benzyloxy-2-(S)-tert-butoxycarbonylamino-butyric acid.     -   DAP or Dap: Diaminopropionate     -   DCM:         4-(Dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4H-pyran     -   DEAD: Diethyl azodicarboxylate     -   DIEA: Diisopropylethylamine     -   DME: 1,2-dimethoxyethane     -   DMF: N,N-Dimethylformamide     -   DMSO: Dimethyl sulfoxide     -   DPPA: Diphenyl phosphoryl azide     -   Et₃N: Triethylamine     -   EDC: N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide     -   EDCI: 1-(3-dimethylaminopropyl)3-ethylcarbodiimide     -   EtOAc: Ethyl acetate     -   EtOH: Ethanol     -   Fmoc: 9-fluorenylmethoxycarbonyl     -   Gly-OH: glycine     -   HATU: O-(7-azabenzotriaazol-1-yl)-N,N,N′N′=tetramethyluronium         hexafluorophophate     -   HBTU: 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium         hexafluorophosphate     -   Hex: hexane     -   HOBt: butyl alcohol     -   HOBT: 1-Hydroxybenzotriazole     -   HPLC: High Pressure Liquid Chromatography     -   IC₅₀ value: The concentration of an inhibitor that causes a 50%         reduction in a measured activity.     -   iPrOH: Isopropanol     -   LC/MS: Liquid Chromatography/Mass Spectrometry     -   LRMS: Low Resolution Mass Spectrometry     -   MeOH: Methanol     -   NaOMe: sodium methoxide     -   nm: Nanometer     -   NMP: N-Methylpyrrolidone     -   PPh₃: triphenyl phosphine     -   RP-HPLC: Reversed-phase high-pressure liquid chromatography     -   RT: Room temperature     -   sat: Saturated     -   TEA: Triethylamine     -   TFA: Trifluoroacetic acid     -   THF: Tetrahydrofuran     -   Thr: Threonine     -   TLC: Thin Layer Chromatography     -   Trt-Br: Tert-butyl bromide

Nomenclature for the Example compounds was provided using ACD Name version 5.07 software (Nov. 14, 2001) available from Advanced Chemistry Development, Inc. Some of the compounds and starting materials were named using standard IUPAC nomenclature.

Synthesis of N-Aroyl Threonine Analogues and Formation of Hydroxamate Example 1 Synthesis of 3-bromo-4-fluoro-N-{(1S,2R)-2-hydroxy-1-[(hydroxyamino) carbonyl]propyl}benzamide (3)

Reagent MW Eq. g/ml mmol Benzoic acid(1) 219.02 1.0 2.152 g 9.83 L-Thr-OMe—HCl 169.61 1.2 1.968 g 11.6 EDCI 191.71 1.2 2.218 g 11.6 HOBt 135.13 1.1 1.410 g 10.4 DIEA 129.25 4.0  6.8 mL 39.0 DMF   60 mL

Preparation of (2S,3R)-2-(3-bromo-4-fluoro-benzoylamino)-3-hydroxy-butyric acid methyl ester (2)

Diisopropylethylamine (6.8 mL, 39.0 mmol) was added to a stirred solution of 3-bromo-4-fluorobenzoic acid 1 (2.152 g, 9.83 mmol), L-threonine methyl ester hydrochloride (1.968 g, 11.6 mmol), EDCI (2.218 g, 11.6 mmol) and HOBt (1.410 g, 10.4 mmol) in anhydrous DMF (60 mL) at 0° C. under N₂. The solution was stirred at 0° C. for 1 h and at room temperature for 20 h. The solution was diluted with EtOAc (300 mL) and washed with 1.0 M HCl (2×80 mL), saturated NaHCO₃ (2×80 mL), H₂O (4×80 mL), dried over MgSO₄, filtered and concentrated in vacuo to give a colorless syrup which solidified on standing to afford 3.280 g (100%) of (2S,3R)-2-(3-bromo-4-fluoro-benzoylamino)-3-hydroxy-butyric acid methyl ester 2 as a white solid, mp 73-74° C. MS (ES+) m/z 333.9 (C₁₂H₁₃BrFNO₄+H requires 334.00).

Preparation of 3-bromo-4-fluoro-N-{(1S,2R)-2-hydroxy-1-[(hydroxyamino)carbonyl]propyl}benzamide (3)

To a solution of hydroxylamine hydrochloride (66 mg, 0.95 mmol) in anhydrous MeOH (2.0 mL) at 0° C. under N₂ atmosphere was added sodium methoxide (25 wt % in MeOH, 360 mg, 1.67 mmol). A precipitate formed immediately and the cloudy white solution was stirred for 10 minutes at 0° C. A solution of methyl (2S,3R)-2-[(3-bromo-4-fluorophenyl)carbonylamino]-3-hydroxybutanoate (2) (284 mg, 0.850 mmol) in MeOH (2.0 mL) was added and the reaction stirred 2 h at 0° C. and then warmed gradually to room temperature overnight (17 h total). Aqueous 1.0 M HCl (10 mL) was added and the solution extracted with 4:1 chloroform/isopropyl alcohol (4×20 mL). The organic layers were combined, dried over Na₂SO₄ and concentrated to give a pink foam. The crude solid was triturated with diethyl ether (2×8 mL) and dried in vacuo to give 3-bromo-4-fluoro-N-{(1S,2R)-2-hydroxy-1-[(hydroxyamino)carbonyl]propyl}benzamide 3 as a white foam: mp 152-153° C. Rf (10:1 CH₂Cl₂/MeOH on silica gel)=0.53.

Preparation of Hydroxamates Example 2 Synthesis of 4-benzoyl-N-{(1S,2R)-2-hydroxy-1-[(hydroxyamino) carbonyl]propyl}benzamide

Procedure:

To a solution of hydroxylamine hydrochloride (121 mg, 1.74 mmol) in anhydrous MeOH (2.0 mL) at 0° C. under N2 atmosphere was added sodium methoxide (25 wt % in MeOH, 680 mg, 3.14 mmol). A precipitate was immediately observed and the cloudy white solution was stirred for 10 minutes at 0° C. A solution of methyl (2S,3R)-3-hydroxy-2-{[4-(phenylcarbonyl)phenyl]carbonylamino}butanoate (1) (534 mg, 1.56 mmol) in MeOH (3.0 mL) was added and the reaction stirred 3 h at 0° C., then warmed gradually to ambient temperature overnight (18 h total). Aqueous 0.5 M HCl (20 mL) was added and the solution extracted with 5:1 chloroform/isopropyl alcohol (4×40 mL). The organic layers were combined, dried over Na₂SO₄ and concentrated to give an orange foam. Purification by silica gel chromatography (increasing eluant polarity from 30:1 CH₂Cl₂/MeOH to 15:1 CH₂Cl₂/MeOH) afforded 228 mg (43%) of 4-benzoyl-N-{(1S,2R)-2-hydroxy-1-[(hydroxyamino) carbonyl]propyl}benzamide.

Example 3 Synthesis of (2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidine-2-carbohydroxamic acid Preparation of ((2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidin-2-yl)-N-(phenylmethoxy)carboxamide (2)

Procedure:

To a solution of (2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidine-2-carboxylic acid (1) (405 mg, 1.27 mmol), benzylhydroxylamine hydrochloride (243 mg, 1.52 mmol), HATU (556 mg, 1.46 mmol), and HOBt (178 mg, 1.32 mmol) in DMF (10 mL) at 0° C. was added diisopropylethylamine (710 mL, 4.07 mmol) with stirring. The cooling bath was removed after one hour and the reaction mixture stirred at ambient temperature for 18 h and then diluted with EtOAc (200 mL). The organic layer was washed with 1.0 M HCl (2×60 mL), sat. NaHCO₃ (2×60 mL) and H₂O (5×60 mL), dried over MgSO₄ and concentrated to give 493 mg (92%) of ((2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidin-2-yl)-N-(phenylmethoxy)carboxamide (2), a colorless oil that slowly crystallized upon standing. Rf (25:1 CH₂Cl₂/MeOH)=0.35.

Preparation of (2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidine-2-carbohydroxamic acid (2)

Procedure:

To a solution of ((2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidin-2-yl)-N-(phenylmethoxy)carboxamide (1) (143 mg, 0.337 mmol) in EtOH (10 mL) was added 20% Pd(OH)₂/C (50 mg). The solution was purged with hydrogen gas (approx. 0.5 L from a 1 L balloon) and then stirred under an atmosphere of H₂ (balloon pressure). TLC analysis showed no starting material after one hour. The solution was diluted with EtOAc (10 mL) and filtered through celite, washing with 20:1 EtOAc/EtOH (50 mL). The solution was concentrated and dried in vacuo to afford 90 mg (80%) of (2R,3R)-3-hydroxy-1-{[4-(trifluoromethoxy)phenyl]carbonyl}pyrrolidine-2-carbohydroxamic acid (2) as a sticky white foam: mp 64-65° C. Rf (10:1 CH₂Cl₂/MeOH)=0.29.

Synthesis of N-Benzyl Threonine Analogues by Reductive Amination Example 4 Synthesis of (2S,3R)-3-hydroxy-2-{[(4-phenylphenyl)methyl]amino}butanehydroxamic acid (3)

Reagent MW Eq. g/ml mmol 4-biphenylcarboxaldehyde 182.22 1.0 1.104 g 6.06 L-Thr-OMe-HCl 169.61 1.0 1.030 g 6.07 NaBH(OAc)₃ 211.94 1.4 1.800 g 8.49 Et₃N 101.19 2.0 1.70 mL 12.1 THF 25 mL

Triethylamine (1.70 mL, 12.1 mmol) was added to a stirred suspension of L-threonine methyl ester hydrochloride (1.030 g, 6.07 mmol) and 4-biphenylcarboxaldehyde (1.104 g, 6.06 mmol) in THF (25 mL). After 20 min, NaBH(OAc)₃ was added and the suspension stirred for 20 h. The reaction was monitored by TLC (50:1 DCM/MeOH, R_(f)=0.4). The reaction mixture was quenched with saturated NaHCO₃ (50 mL), extracted with EtOAc (2×120 mL), dried over MgSO₄, filtered and concentrated to give a yellow oil. Purification by silica gel chromatography (150:1 DCM/MeOH) afforded 1.220 g (67% yield, 98% pure) of (2S,3R)-2-[(biphenyl-4-ylmethyl)-amino]-3-hydroxy-butyric acid methyl ester 2 as a pale yellow oil.

HPLC (260 nm, 34 min run) 14.2 min; LRMS (ES+) m/z 299.9 (C₁₈H₂₁NO₃+H requires 300.10). Compound 3 was then formed by the addition of NH₂OH in MeOH/NaOMe at 0° C., warming to ambient temperature of the period of several hours. LCMS MH+ 301.15.

General Methods for Making Phenyl-benzoic acids and Phenyl-benzoate esters (see Example 5 below)

Suzuki Procedures Using Pd(dppf)C₁₂-DCM Catalyst and a THF/H₂O Mixture

Reagent MW EQ g/ml mmol BromoArene #1 ~300 1  100 mg ~0.33 Boronic Acid #2 — 1.2 — ~0.40 Na₂CO₃ 105.99 3  104 m ~0.99 Pd(dppf)Cl₂ 816.63 0.1-0.2 27-54 mg ~0.033-0.066 THF (3) (sparged with argon for 5 min.)   0.75 ml water(1) (sparged with argon for 5 min.)   0.25 ml Standard Procedure

1 eq aryl halide (1) was added to 1.2 eq. (2) and Pd(dppf)Cl₂ in THF, followed by addition of water and stirred 8 hours at RT. Upon completion (usually over night), the reactions are diluted with ethyl acetate (5-10 ml) and water (1 ml). The organic layer is separated and washed with NaHCO₃ (2×3 ml), water (1×3 ml), brine (1×3 ml), dried with Na₂SO₄, filtered and concentrated in an 8 ml glass vial. The residue is dissolved in DMSO and injected on a preparatory HPLC reverse phase column to afford >80% yield.

Suzuki Procedures Using Pd(dppf)C₁₂-DCM Catalyst and DMF Solvent

Reagent MW EQ g/ml mmol BromoArene #1 ~500 1  20 mg ~0.04 Boronic Acid #2 ~200 2 ~14 mg ~0.08 Pd(dppf)Cl₂ 816.63 0.25  10 mg ~0.01-0.02 TEA 101.19 5  28 μL ~0.2 DMF (dry & sparged with argon for 5 min.)  0.5 ml Standard Procedure

The haloarene 1 and boronic acid 2 were weighed out and placed in the reaction flask. The DMF was sparged with argon for 5-10 minutes, followed by TEA addition, and the reaction was lightly bubbled with argon. The solid Pd(dppf)Cl₂ catalyst was added in one portion. The vial was flushed with argon, capped tight and stirred or shaken at ˜80° C. Upon reaching completion (over night), the reaction was filtered and injected on a preparatory HPLC reverse phase column (80% yield).

Synthesis of Methyl DAP Analogues Example 5 3-(R)-Amino-2-(S)-[(4′-ethyl-biphenyl-4-carbonyl)-amino]-butyl-hydroxamic acid (8)

Preparation of N-triphenylmethyl allo-threonine methyl ester (2)

Reagent MW EQ g/ml mmol H-allo-Thr-OMe•HCl (1) 169.7 1.2  2.0 g 12.0 Trt-Br 323.24 1.0 3.23 g 10.0 DIEA 129.25 3.0  5.2 ml 30.0 CHCl₃ (dry)  100 ml

For similar procedures see: Righi, P.; Scardovi, N.; Marotta, E.; ten Holte, P.; Zwanenburg, B. Organic Letters 2002, 4(4), 497-500.

A solution of trityl bromide (3.2 g, 10.0 mmol) in CHCl₃ (40 ml) was added dropwise to a stirred solution of allo-threonine methyl ester HCl salt (1) (2.0 g, 12.0 mmol) and DIEA (5.2 ml, 30.0 mmol) in CHCl₃ (60 ml) at rt under N₂. The reaction could be followed by TLC eluting with EtOAc/Hex (40:60) (Rf=0.3). After stirring 12 h, the reaction was concentrated to a brown oil. The crude product was diluted with EtOAc (170 ml) and washed with 0.2 N citric acid (2×50 ml), water (2×50 ml), brine (50 ml), dried (Na₂SO₄), filtered and concentrated under reduced pressure to yield 3.73 g (85% yield, 95% pure) of a yellow solid.

HPLC (220 nm, 41 min. run) 30.90 min.; HPLC (220 nm, 17 min. run) 14.86 min.; LCMS: LC (214 nm) 3.06 min., MS (ES+) m/z 376.2 (C₂₄H₂₅NO₃+H requires 376.18).

Preparation of 3-(R)-Azido-2-(S)-(trityl-amino)-butyric acid methyl ester (3)

Reagent MW Eq. g/ml mmol Trt-allo-Thr-OMe (2) 375.46 1.0 4.08 g 10.88 PPh₃ 262.29 1.0 2.85 g 10.88 DEAD (neat) 174.16 1.6 2.93 ml 17.82 DPPA 275.7 2.7 6.40 ml 29.7 THF (dry)   50 ml

For similar procedures see: Matsuda, A.; Yasuoka, J.; Sasaki, T.; Ueda, T. J. Med. Chem. 1991, 34, 999-1002.

A solution of pure DEAD (2.9 ml, 17.8 mmol) in THF (5 ml) was added slowly dropwise to a stirred solution of trt-allo-threonine methyl ester (2) (4.1 g, 10.9 mmol) and PPh₃ (2.9 g, 10.9 mmol) in THF (40 ml) at 0° C. under N₂. After 3 min., a solution of DPPA (6.4 ml, 29.7 mmol) in THF (5 ml) was added to the orange-yellow reaction solution at 0° C. After 1 h, the reaction was allowed to warm to rt. After 40 h, the reaction had reached completion by TLC (Hexane/DCM/EtOAc (64:20:16) (Rf=0.6)) and LCMS. The yellow solution was concentrated to give 18 g of crude material that was purified by column chromatography eluting with Hexane/EtOAc (88:12) giving 3.5 g of 70% pure product after evaporation. The product was purified again (to remove trityl alcohol and a crotyl side-product formed during the reaction by elimination) by column chromatography eluting with Hexane/DCM/EtOAc (76:20:4) giving 1.65 g (38% yield) of a pale yellow oil after concentration and drying in vacuo. Note that the trityl protecting group would hydrolyze when exposed to TFA while running the sample on HPLC.

Alternately, the reaction could be carried out in dry DCM. A reaction using 5.44 g (14.5 mmol) of trt-allo-threonine methyl ester (2) in DCM (100 ml) with PPh₃ (3.8 g, 14.5 mmol), pure DEAD (3.4 ml, 21.8 mmol) in DCM (5 ml) and DPPA (6.3 ml, 24.0 mmol) in DCM (10 ml) were combined following the procedure above. After 3 days, the reaction did not progress further by TLC and LCMS. After the same work up, 2.97 g of the product was obtained in 51% yield.

HPLC (220 nm, 41 min. run) 40.5 min.; HPLC (220 nm, 17 min. run) 16.32 min.; LCMS: LC (214 nm) 3.7 min., MS (ES+) m/z 401.2 (C₂₄H₂₅N₃O₂+H requires 401.15).

Preparation of 2-(S)-Amino-3-(R)-azido-butyric acid methyl ester HCl Salt (4)

Reagent MW EQ g/ml mmol Trt-Azido-Thr-OMe (3) 400.47 1.0 4.79 g 11.98 TFA   57 ml CHCl₃ (dry)   3 ml

A solution of Trt-Azido-Thr-OMe (3) (4.8 g, 12.0 mmol) was dissolved in a 95% TFA/DCM solution (60 ml) at rt with stirring. After 2.5 h, the reaction was complete by LCMS. The bright yellow solution was diluted with 0.5 N aq. HCl (300 ml). The aqueous layer was extracted with DCM (2×30 ml) and then lyophilized to dryness. The white solid was dissolved in AcCN/water (50:50) (100 ml) and again lyophilized to dryness to produce a consistent powder and remove as much of the TFA as possible. The azido-Thr product (4), 2.26 g (97% yield, 95% pure) of a white solid, was obtained as the HCl salt.

HPLC (220 nm, 41 min. run) 7.91 min.; HPLC (220 nm, 17 min.run) 3.36 min; LCMS: LC (214 nm) 0.48 min., MS (ES+) m/z 159.3 (C₅H₁₀N₄O₂+H requires 159.08).

Preparation of 3-(R)-Azido-2-(S)-[(4′-ethyl-biphenyl-4-carbonyl)-amino]-butyric acid methyl ester (6)

Reagent MW EQ g/ml mmol Azido-Thr-OMe•HCl (4) 194.62 1.0  195 mg 1.0 Biphenyl Acid (5) 226.27 1.0  226 mg 1.0 HOBT 153 1.0  158 mg 1.0 EDC•HCl 191.17 1.3  249 mg 1.3 DIEA 129.25 2.5 0.44 ml 2.5 DCM (dry)   10 ml

A EDC-HCl (249 mg, 1.3 mmol) was added to a stirred colorless solution of azido-Thr-OMe-HCl (4) (195 mg, 11.0 mmol), HOBT (158 mg, 11.0 mmol), 4′-Ethyl-biphenyl-4-carboxylic acid (5) (226 mg, 1.0 mmol) and DIEA (0.44 ml, 2.5 mmol) in DCM (10 ml) at rt under N₂. After 24 h, the reaction had reached completion by TLC (Hexane/EtOAc (60:40) (Rf=0.3)) and LCMS. The reaction was evaporated under reduced pressure to a brown tar. The crude product was dissolved in EtOAc (100 ml) and washed with 0.2N aq. HCl (2×50 ml), aq. sat. NaHCO₃ (50 ml), brine (50 ml), dried (Na₂SO₄), filtered and concentrated under reduced pressure to yield a crude brown solid. The crude material was further purified by column chromatography eluting with Hexane/EtOAc (70:30) giving 245 mg (67% yield) of pure product after evaporation and drying in vacuo.

HPLC (220 nm, 41 min. run) 33.87 min.; HPLC (220 nm, 17 min. run) 15.61 min; LCMS: LC (214 nm) 3.25 min., MS (ES+) m/z 367.2(C₂₀H₂₂N₄O₃+H requires 367.17).

Preparation of 3-(R)-Amino-2-(S)-[(4′-ethyl-biphenyl-4-carbonyl)-amino]-butyric acid methyl ester (7)

Reagent MW EQ g/ml mmol Biphenyl Azido-Thr (6) 366.41 1.0 244 mg 0.67 10% Pd/C 200 mg H₂ (gas) 12″ balloon MeOH (dry)  10 ml

A solution of biphenyl azido-Thr methyl ester (6) (244 mg, 0.67 mmol) in MeOH (10 ml) was made by sonicating until the milky precipitate cleared. After bubbling nitrogen through the reaction solution for 30 sec., 10% Pd/C was added in one portion. The reaction was stirred under nitrogen at RT. The reaction was exposed to aspirator vacuum to remove the nitrogen and then opened to the hydrogen gas at balloon pressure (˜1 atm). The reaction stirred for 3 h at which time the hydrogen was exchanged for nitrogen. The reaction was filtered through a pad of celite to remove the palladium. The celite pad was washed with MeOH (30 ml). The combined fractions of MeOH were evaporated under reduced pressure and dried in vacuo to give 225 mg (99% yield) of pure produce (7) as a white solid.

HPLC (220 nm, 17 min. run) 10.79 min.; LCMS: LC (214 nm) 2.21 min., MS (ES+) m/z 341.2 (C₂₀H₂₄N₂O₂+H requires 341.18).

Preparation of 3-(R)-Amino-2-(S)-[(4′-ethyl-biphenyl-4-carbonyl)-amino]-butyl-hydroxamic acid (8)

Reagent MW EQ g/ml mmol Amino-Thr-OMe (7) 340.42 1.0   225 mg 0.66 H₂NOH•HCl 69.49 10.0   460 mg 6.6 NaOMe 54.02 ~12.0 ~430 mg 7.92 MeOH (dry)    7 ml DCM (dry)    5 ml

To a stirred suspension of biphenyl-amino-Thr methyl ester (7) (225 mg, 0.6 mmol) and hydroxylamine HCl salt (460 mg, 6.6 mmol) in MeOH (7 ml) and DCM (5 ml) was added fresh solid NaOMe powder (430 mg, 7.92 mmol) in one portion. After stirring for 2 min. at rt under nitrogen, the pH of the reaction on wet pH paper was approximately 7-8. The suspension had change from larger particles of white solid to a finely-divided milky consistency. The pH of the reaction was checked after adding small portions of NaOMe (50-100 mg) and allowing 2 min. for the reaction to equilibrate. The pH of the reaction reached a stable 11-12 after the final portion of NaOMe was added (250 mg total). The reaction was initiated at pH 11 and proceeded quickly. After 30 min., the reaction reached 85% completion as determined by LCMS, and the reaction was placed in a −10° C. bath. The cold mixture filtered over fine filter paper on a Büchner funnel. The white residue was washed with MeOH (15 ml). The organic fractions were collected and concentrated under reduced pressure to give crude product (750 mg). The crude product (only one 150 mg portion) was dissolved in DMSO (1 ml), AcCN (100 μl) and water (100 μl), passed through a Teflon syringe filter, and the clear filtrate was injected on a preparative HPLC. The purification used a 20×50 mm Ultro 120 C18 column running a 22 ml/min 2% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness. The product as the TFA salt was dissolved in AcCN/water (50:50) (5 ml), 1N aq. HCl (1 equivalent) and lyophilized again to give 11.5 mg of white powder as an HCl salt (23% yield).

HPLC (220 nm, 41 min. run) 19.31 min.; HPLC (220 nm, 17 min. run) 9.39 min; LCMS: LC (214 nm) 1.98 min., MS (ES+) m/z 342.2 (C₁₉H₂₃N₃O₃+H requires 342.17).

Synthesis of 4′Benzamide Biphenyl Threonine Hydroxamic Acid Example 6 Biphenyl-4,4′-dicarboxylic acid 4′-[(3-Boc-amino-propyl)-amide]-4-[((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-amide](6), and Example 7 Biphenyl-4,4′-dicarboxylic acid 4′-[(3-amino-propyl)-amide]4-[((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-amide](7)

Synthesis of (2S,3R)-2-amino-3-(phenylmethoxy)-N-(phenylmethoxy)butanamide (1)

Procedure:

To a suspension of benzylhydroxylamine hydrochloride (8.310 g, 52.06 mmol), Boc-Thr(OBn)-OH (14.01 g, 45.28 mmol), EDCI (10.01 g, 52.21 mmol), and HOBt (6.90 g, 51.06 mmol) in CH₂Cl₂ (300 mL) at 0° C. was added diisopropylethylamine (28.3 mL, 162 mmol) with stirring. The cooling bath was removed after one hour and the reaction mixture stirred at ambient temperature for 20 h and was then diluted with CH₂Cl₂ (300 mL). The organic layer was washed with 1.0 M HCl (2×200 mL), sat. NaHCO₃ (2×200 mL) and brine (200 mL), dried over MgSO₄ and concentrated to give 14.5 g of a white solid. The crude solid was treated with a solution of trifluoroacetic acid (90 mL) in CH₂Cl₂ (90 mL) and stirred for 2.5 h. The reaction mixture was concentrated by rotary evaporation and then diluted with CH₂Cl₂ (600 mL). The organic layer was washed with sat. NaHCO₃ (2×200 mL), dried over MgSO₄ and concentrated to give a dark orange oil. Purification by silica gel chromatography (50:1 CH₂Cl₂/MeOH) afforded (2S,3R)-2-amino-3-(phenylmethoxy)-N-(phenylmethoxy) butanamide (A) (8.9 g,) as a pale yellow oil. Rf (50:1 CH₂Cl₂/MeOH on silica gel)=0.2.

Preparation of (1S,2R)-4′-(2-benzyloxy-1-benzyloxycarbamoyl-propylcarbamoyl)-biphenyl-4-carboxylic acid (3)

Reagent MW Eq. g/mL mmol Amine (1) 314.38 1.0 0.944 g 3.00 Dicarboxylic acid (2) 242.23 1.9 1.360 g 5.61 BOP 442.3 1.5 2.007 g 4.54 DIEA 129.25 3.3 1.7 mL 9.76 DMF 200 mL

To a suspension of 4,4′-biphenyldicarboxylic acid 2 (1.360 g, 5.61 mmol) in DMF (180 mL) was added BOP (2.007 g, 4.54 mmol) and DIEA (1.7 mL, 9.8 mmol). A solution of (1S,2R)-2-amino-3,N-bis-benzyloxy-butyramide 1 (944 mg, 3.00 mmol) in DMF (20 mL) was added and the reaction stirred for 18 h. The solution was diluted with EtOAc (250 mL) and washed with 1.0 M HCl (500 mL). The aqueous layer was extracted with EtOAc (250 mL) and the organic layers combined. The organic layer was washed with 1.0 M HCl (250 mL), dried over MgSO₄, and concentrated to give a crude yellow solid. Purification by silica gel chromatography (60:1 CH₂Cl₂/MeOH) gave 210 mg (1S,2R)-4′-(2-benzyloxy-1-benzyloxycarbamoyl-propylcarbamoyl)-biphenyl-4-carboxylic acid 3. (13% yield) as a yellow solid. R_(f)=0.80 (10:1 CH₂Cl₂/MeOH); LRMS (ES+) m/z 539.1 (C₃₂H₃₀N₂O₆+H requires 539.22).

Preparation of biphenyl-4,4′-dicarboxylic acid 4′-[(3-(Boc)-amino-propyl)-amide]-4-[(2R)-benzyloxy-(1S)-benzyloxycarbamoyl-propyl)-amide] (5)

Reagent MW Eq. g/mL mmol Biphenylcarboxylic acid (3) 538.59 1.0 0.200 g 0.371 Amine (4) 174.24 1.1 0.071 g 0.407 EDCI 191.71 1.1 0.078 g 0.407 HOBt 135.13 1.0 0.052 g 0.385 DIEA 129.25 2.7 180 μL 1.0 DMF 2 mL

To a solution of biphenylcarboxylic acid 3 (200 mg, 0.371 mmol), EDCI (78 mg, 0.407 mmol), and HOBt (52 mg, 0.385 mmol) in DMF (2 mL) was added t-Butyl N-(3-aminopropyl)carbamate 4 (71 mg, 0.407 mmol) and DIEA (180 μL, 1.0 mmol). The reaction mixture was stirred 24 h, diluted with EtOAc (150 mL), washed with 1.0 M HCl (2×60 mL), saturated NaHCO₃ (2×60 mL), H₂O (3×60 mL), dried over MgSO₄ and concentrated to give a crude white solid. Purification by silica gel chromatography (25:1 CH₂Cl₂/MeOH) afforded 194 mg (75% yield) of biphenyl-4,4′-dicarboxylic acid 4′-[(3-(Boc)-amino-propyl)-amide]-4-[(2R)-benzyloxy-(1S)-benzyloxycarbamoyl-propyl)-amide] 5 as a white solid. R_(f)=0.15 (50:1 CH₂Cl₂/MeOH); LRMS (ES+) m/z 695.2 (C₄₀H₄₆N₄O₇+H requires 695.35).

Preparation of Biphenyl-4,4′-dicarboxylic acid 4′-[(3-Boc-amino-propyl)-amide]-4-[((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-amide](6)

Reagent MW Eq. g/mL mmol Biphenyl diamide (5) 694.82 1.00 0.190 g 0.273 Pd(OH)₂ (20%/C) 106.42 0.15 0.020 g 0.040 H₂ (g) balloon THF 5.0 mL MeOH 3.0 mL

A solution of dibenzyl-protected threonine hydroxamic acid 5 (190 mg, 0.273 mmol) in THF (5 mL) and MeOH (3 mL) was charged with Pd(OH)₂ (20%/C, 20 mg, 0.04 mmol) and stirred under a hydrogen atmosphere (balloon pressure) for 16 h. The crude mixture was filtered through a plug of celite eluting with 2:1 MeOH/THF (15 mL) and concentrated to give an orange syrup. Purification by silica gel chromatography (5:1:1 THF/MeOH/CH₂Cl₂ afforded 110 mg (78% yield) of biphenyl-4,4′-dicarboxylic acid 4′-[(3-Boc-amino-propyl)-amide]-4-[((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-amide] as a white foam, mp 75-77° C. R_(f)=0.20 (10:1 CH₂Cl₂/MeOH); LRMS (ES+) m/z 515.4 (C₂₆H₃₄N₄O₇+H requires 515.26).

Preparation of Biphenyl-4,4′-dicarboxylic acid 4′-[(3-amino-propyl)-amide]-4-[((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-amide] (7)

Reagent MW Eq. g/mL mmol Boc-protected amine (6) 514.57 1.00 0.080 g 0.155 TFA 3.0 mL CH₂Cl₂ 3.0 mL

A flask containing Boc-protected amine 6 (80 mg, 0.155 mmol) was treated with 50% TFA/CH₂Cl₂ (6.0 mL) and stirred for 2.5 h. The reaction mixture was concentrated by rotary evaporation to give a brown syrup. Purification by RP-HPLC(C₁₈ column, CH₃CN gradient 5-70%, 0.1% TFA, UV analysis 300 nm, 36 min) and lyophilization of the collected fractions afforded 14 mg (21% yield) of biphenyl-4,4′-dicarboxylic acid 4′-[(3-amino-propyl)-amide]-4-[((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-amide] as a white solid. LRMS (ES+) m/z 415.3 (C₂₁H₂₆N₄O₅+H requires 415.20); RP-HPLC (300 nm, 36 min run) 18.2 min.

Example 8 Synthesis of N-(2-(N-hydroxycarbamoyl)(2S)-2-{[4-(4-ethylphenyl)phenyl]carbonylamino}ethyl)acetamide (4)

Preparation of 3-Acetylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid (2)

Reagent MW EQ g/ml mmol Fmoc-DAP-H (1) 326.4 1.0 980 mg 3.0 Acetic anhydride 102.09 1.5 425 uL 4.5 Pyridine 79.1 2.0 483 uL 6.0 THF  20 ml

Acetic anhydride in THF (5 ml) was added to a cloudy mixture of Fmoc-DAP-H (1) (980 mg, 3.0 mmol) and pyridine (483 uL, 6.0 mmol) in THF (15 ml) with stirring at rt. After 4 hours, the clear pale yellow solution had reacted completely by LCMS. The reaction was evaporated under reduced pressure. The residue was dissolved in EtOAc (150 ml) and washed with 0.1M NaHSO₄ (50 ml), water (50 ml), sat. brine (50 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure to give 1.1 g of crude product as a white solid. The crude product was purified by prep. HPLC to give 0.99 g (90% yield) of acyl-DAP (2).

Preparation of (2-Acetylamino-1-hydroxycarbamoyl-ethyl)-carbamic acid 9H-fluoren-9-ylmethyl ester trityl resin (3)

Reagent MW EQ g/ml mmol H₂N—O-Trt Resin 1.0   120 mg 0.113 Fmoc-DAP(Ac)-H (1) 368.4 5.0   980 mg 0.564 HATU 380 5.0 0.146 g 0.564 DIEA 129.25 10.0   196 ul 1.13 NMP  1.7 ml

A solution of Fmoc-DAP(Ac)-H (1) (980 mg, 0.56 mmol), HATU (0.146 g, 0.56 mmol) in NMP (1.7 ml) was made. After 2 min. of shaking, the activated acid was added to the deprotected H₂N—O-Trt Resin (120 mg, 0.113 mmol) at rt with shaking. [Deprotection of the Fmoc group from the resin was accomplished using 20% piperizine in DMF (4 ml) for 2 hours twice. The resin was drained and washed with DMF (2×5 ml) and DCM (2×5 ml).] After shaking for 20 hours, the reaction was drained and washed with DMF (2×5 ml) and DCM (2×5 ml). The resin was dried and used as is in the next reaction.

Preparation of N-(2-(N-hydroxycarbamoyl)(2S)-2-{[4-(4-ethylphenyl)phenyl]carbonylamino}ethyl)acetamide (4) Preparation of (2-Acetylamino-1-hydroxycarbamoyl-ethyl)-carbamic acid 9H-fluoren-9-ylmethyl ester trityl resin (3)

Reagent MW EQ g/ml mmol Fmoc-DAP(Ac)-Trt Resin (3) 1.0 120 mg 0.113 4′-Etbiphenyl-4-carboxy acid 226.3 5.0  91 mg 0.4 HATU 380 5.0 152 mg 0.4 DIEA 129.25 10.0 140 ul 0.8 NMP  1.0 ml

The resin was treated with 20% piperizine in DMF (4 ml) for 2 hours twice. The resin was drained and washed with DMF (2×5 ml) and DCM (2×5 ml). The resin was dried in vacuo. A solution of 4′-Ethyl-biphenyl-4-carboxylic acid (91 mg, 0.4 mmol), HATU (152 g, 0.4 mmol) in NMP (1.0 ml) was made. After 2 min. of shaking, the activated acid was added to the deprotected H-DAP(Ac)-Trt resin (120 mg, 0.113 mmol) at rt with shaking. After shaking for 18 hours, the reaction was drained and washed with DMF (2×5 ml) and DCM (2×5 ml). The resin was dried in vacuo. The product was cleaved from the resin through treatment with a solution of TFA (500 uL), DCM (500 uL) and water (50 uL) for 25 min. The resin was filtered and washed with fresh DCM (2 ml). The combined TFA and DCM fractions are evaporated under reduced pressure. The residue was diluted with CH₃CN/water (1:1) (10 ml) and lyophilized. The crude product was purified by prep. HPLC. The crude product was dissolved in DMSO (1 ml), passed through a Teflon syringe filter, and the clear filtrate was injected on a preparative HPLC. The purification used a 20×50 mm Ultro 120 C18 column running a 22 ml/min 2% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness. The solid residue was lyophilized again from CH₃CN/water (1:1) (5 ml) give 8.6 mg of pure product (4) (˜21% yield).

Example 9 Synthesis of 4′-Ethyl-biphenyl-4-carboxylic acid (1-hydroxycarbamoyl-2-methanesulfonylamino-ethyl)-amide (3) Preparation of 4′-Ethyl-biphenyl-4-carboxylic acid (2-amino-1-hydroxycarbamoyl-ethyl)-amide trityl resin (2)

Reagent MW EQ g/ml mmol Biphenyl-DAP(Alloc)-Trt Resin (1) 1.0  500 mg 0.35 Dimethyl barbituric acid 156.14 10.0  600 mg 3.5 Pd(PPh₃)₄ 1135.6 1.0  438 mg 0.35 PPh₃ 262.3 2.0  202 mg 0.7 DCM 11.0 ml

Pd(PPh₃)₄ (438 mg, 0.35 mmol) was added to a vial containing biphenyl-DAP(Alloc)-Trt Resin (1) (500 mg, 0.35 mmol), Dimethyl barbituric acid (600 mg, 3.5 mmol) and PPh₃ (438 mg, 0.35 mmol) in DCM (11 ml) at rt under argon. The mixture was sparged with argon and shaken for 16 hours. The bright yellow mixture was drained and washed with DMF (8×10 ml) and DCM (8×10 ml). The resin was dried in vacuo to give the deprotected DAP resin 2.

Preparation of 4′-Ethyl-biphenyl-4-carboxylic acid (1-hydroxycarbamoyl-2-methane sulfonylamino-ethyl)-amide (3)

Reagent MW EQ g/ml mmol Biphenyl-DAP-Trt Resin (2) 1.0  160 mg 0.11 Methanesulfonyl chloride 114.55 10.0   85 uL 1.1 Lutidine 107.16 15.0  190 uL 1.6 DCM  1.5 ml

Methanesulfonyl chloride (85 uL, 1.1 mmol) was added to a mixture of deprotected DAP resin (2) (160 mg, 0.11 mmol) and lutidine (190 uL, 1.6 mmol) in DCM (1.5 ml). After shaking for 16 hours, the mixture was drained and washed with DMF (10×2 ml) and DCM (5×2 ml). The product was cleaved from the resin through treatment with TFA/water (4:1) (1.5 ml). After shaking for 45 min., the TFA solution was collected from the resin by filtration, and the resin was washed with TFA (1 ml) and TFA/water (1:1) (10 ml). The combined TFA fractions were concentrated under reduced pressure to a reddish-brown solid. The product, identified by LCMS, was purified by prep. HPLC using a 20×50 mm Ultro 120 C18 column running a 22 ml/min 4% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness. The solid residue was lyophilized again from CH₃CN/water (1:1) (5 ml) give 4 mg of pure product as a white solid (3) (˜9% yield).

Example 10 Synthesis of 41-Ethyl-biphenyl-4-carboxylic acid [2-(3,3-dimethyl-ureido)-1-hydroxycarbamoyl-ethyl]-amide (3) (Continued from compound 2 of Example 9 above)

Reagent MW EQ g/ml mmol Biphenyl-DAP-Trt Resin (2) 1.0 125 mg 0.096 Dimethylcarbamyl chloride 107.5 10.0 103 mg 0.96 Lutidine 107.16 20.0 225 uL 1.92 DCM 1.5 ml

Dimethylcarbamyl chloride (103 mg, 0.96 mmol) was added to a mixture of deprotected DAP resin (2) (125 mg, 0.096 mmol) and lutidine (225 uL, 1.92 mmol) in DCM (1.5 ml). After shaking at rt for 5 hours, the mixture was drained and washed with DCM (5×2 ml), DMF (5×2 ml) and DCM (5×2 ml). The product was cleaved from the resin through treatment with TFA/water (4:1) (1.5 ml). After shaking for 45 min., the TFA solution was collected from the resin by filtration, and the resin was washed with TFA/water (1:1) (2 ml). The combined TFA fractions were concentrated under reduced pressure to a reddish-brown solid. The product, identified by LCMS, was purified by prep. HPLC using a 20×50 mm Ultro 120 C18 column running a 22 ml/min 4% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness. The solid residue was lyophilized again from CH₃CN/water (1:1) (5 ml) give 5 mg of pure product as a white solid (3) (˜13% yield).

Example 11 Synthesis of 4′-Ethyl-biphenyl-4-carboxylic acid [2-(2-amino-ethylamino)-1-hydroxycarbamoyl-ethyl]-amide (2)

Reagent MW EQ g/ml mmol Biphenyl-DAP-hydroxamate (1) 327.4 1.0 20 mg 0.096 Boc-amino-acetaldehyde 159.19 4.0 6.4 mg 0.4 NaBH₃CN 62.84 10.0 3.1 mg 0.05 Acetic acid 60.05 20.0 6 uL 1.00 DCM 1.5 ml

NaBH₃CN (3.1 mg, 0.05 mmol) followed by acetic acid (6 uL, 1.0 mmol) were sequentially added to a stirred suspension of biphenyl-DAP-hydroxamate (1) (20 mg, 0.096 mmol) and Boc-amino-acetaldehyde (6.4 mg, 0.4 mmol) in MeOH (1.5 ml) in a 4 ml vial. The reaction was followed by LCMS. After stirring 12 hours, the cloudy reaction was only 50% complete. The reaction was concentrated under reduced pressure to a thick slurry that was dissolved in DMSO. The product was purified by prep. HPLC using a 20×50 mm Ultro 120 C18 column running a 22 ml/min 3% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness. The dried powder was dissolved in CH₃CN/water (1:1) (1 ml) and 1M HCl (700 uL). After heating at 50° C. for 75 min., the reaction mixture was again lyophilized to dryness to produce 7.1 mg of product (2) as a 2× HCl salt white powder (˜17% yield).

Example 12 Synthesis of N-(1-(N-hydroxycarbamoyl)(1S,2R)-2-hydroxypropyl) [4-(2-phenylethynyl)phenyl]carboxamide

Preparation of 4-Phenylethynyl-benzoic acid (3)

Reagent MW EQ g/ml mmol Iodo-benzoate 1 262 1.0 20.0 g 76.34 Ethynyl-benzene 2 102 1.1 8.56 g 83.96 PdCl₂(PPh₃)₂ 702 0.012 0.65 g 0.92 CuI 190 0.024 0.35 g 1.83 TEA 101 1.5 16 ml 114.5 d = 0.726 THF (dry & sparged with argon for 5 110 ml min.)

The 4-iodo-benzoic acid methyl ester 1 (20.0 g, 76.34 mmol), ethynyl-benzene 2 (8.56 g, 83.96 mmol), PdCl₂(PPh₃)₂ (0.65 g, 0.92 mmol), and CuI (0.35 g, 1.83 mmol) were mixed with THF (110 ml) in a round bottom under argon. The dry THF was sparged with dry, oxygen-free argon for at least 5 min. immediately before use. The reaction was cooled to 10° C. and TEA (16 ml) was added. The cooling bath was removed and the reaction was stirred at RT under argon. After 2.5 h, the reaction was diluted with EtOAc (400 ml) and the solids were filtered off through a pad of celite. The organic filtrate was washed with 1M HCl (60 ml), sat. aq. NaHCO₃ (60 ml), water (60 ml), brine (60 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure. The crude solid methyl ester was dissolved in MeOH (400 ml), 6M NaOH (30 ml) and water (50 ml). The reaction was stirred at 70° C. until a clear solution was formed (about 1 h). The reaction could be followed by LCMS. The reaction was cooled and diluted with water (500 ml) and hexane (100 ml). The pH was adjusted to pH 6-7. The white solid that formed was collected and washed with water (3×60 ml) and hexane (3×60 ml). The solid 3 was dried in vacuo yielding 17.3 g (approximately quantitative yield in 99% purity).

Preparation of 3-Hydroxy-2-(4-phenylethynyl-benzoylamino)-butyric acid methyl ester (4)

Reagent MW EQ g/ml mmol 4-Phenylethynyl-benzoic acid (3) 222 1.0 1.55 g 7.0 Threonine methyl ester•HCl 169.65 1.4 1.66 g 9.8 HBTU 380 1.0 2.66 g 7.0 DIEA 125.28 2.5 3.05 ml 17.5 DMF 21 ml

A solution of threonine (1.66 g, 9.8 mmol) and DIEA (1.53 ml, 8.8 mmol) in DMF (10 ml) was added to a stirred solution of 4-phenylethynyl-benzoic acid 3 (1.55 g, 7.0 mmol) and DIEA (1.53 ml, 8.8 mmol) in DMF (11 ml) at rt. After 12 h, the reaction was diluted with EtOAc (300 ml) and washed with 0.5M HCl (2×60 ml), sat. aq. NaHCO₃ (60 ml), 50% diluted brine (60 ml), sat. brine (60 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure. Upon drying in vacuo, 2.34 g of white solid was obtained (approximately quantitative yield in 99% purity).

Preparation of N-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-phenylethynyl-benzamide (5)

Reagent MW EQ g/ml mmol Tolanoic-Thr-OMe (4) 340.42 1.0 2.34 g 7.0 H₂NOH·HCl 69.49 10.0 4.81 g 70.0 NaOMe 54.02 >11.0 >4.16 g >77.0 MeOH (dry) 50 ml DCM (dry) 30 ml

A solution of tolanoic-Thr methyl ester (4) (2.34 g, 7.0 mmol) in MeOH (20 ml) and DCM (30 ml) was added to a cooled (−10° C. bath) suspension of hydroxylamine HCl salt (4.81 g, 70.0 mmol) and NaOMe (4.16 g, 77.0 mmol) in MeOH (30 ml). Follow reaction by LCMS. After stirring for 2 hours, the reaction seems to stall at 50% completion. Add an additional 1 equivalent of NaOMe (0.416 g). After 3 hours, the reaction was 75% complete. Add an additional 0.5 equivalent of NaOMe (0.21 g). After 4 hours, the reaction was 90% complete. Add an additional 0.15 equivalent of NaOMe (0.064 g) for a total of 12.65 equivalents of NaOMe. The pH of the reaction was between 11-12 and had reacted about 95% completion. The reaction was diluted with EtOAc (500 ml) and washed with sat. aq. NaHCO₃ (2×60 ml), 50% diluted brine (60 ml), sat. brine (60 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure. The residue was dissolved in minimal DMA. The product was purified by prep. HPLC using a reverse phase Ultro 120 C18 column running a 2% gradient (AcCN/water, 0.1% TFA). The purified fractions were lyophilized to dryness. The product as the TFA salt was dissolved in AcCN/water (50:50) (80 ml), 1N aq. HCl (13 equivalent) and lyophilized again to give 1.3 g of white powder in 55% yield and >97% purity.

Example 13 Synthesis of 3-(R)-Amino-2-(S)-(3-phenylethynyl-benzoylamino)-butyl-hydroxamic acid (10) Preparation of 3-(R)-Azido-2-(S)-(3-phenylethynyl-benzoylamino)-butyric acid methyl ester (9)

The synthesis of compound 4 is described above. The tolanyl compound (9) was made by the same procedures as for compound (6). The product (9) was obtained in 92% yield (952 mg).

HPLC (220 nm, 41 min. run) 32.64 min.; HPLC (220 nm, 17 min. run) 15.08 min LCMS: LC (214 nm) 3.16 min., MS (ES+) m/z 363.1 (C₂₀H₈N₄O₃+H requires 363.14).

Preparation of 3-(R)-Amino-2-(S)-(3-phenylethynyl-benzoylamino)-butyl-hydroxamic acid (10)

Reagent MW Eq. g/ml mmol Amino-Thr-OMe (9) 362.38 1.0 726 mg 2.0 PPh₃ 262.29 1.0 526 mg 2.0 H₂NOH•HCl 69.49 10.0 1.4 g 20.0 NaOMe 54.02 ~12.0 1.3 g 24.0 THF (dry) 20 ml MeOH (dry) 20 ml

Triphenylphosphine (526 mg, 2.0 mmol) was added to a stirred solution of tolanyl-azido-Thr methyl ester (9) (726 mg, 2.0 mmol) at rt. After 3 days the reaction reached completion as judged by TLC (EtOAc/Hex (2:1)) and LCMS. The reaction was concentrated under reduced pressure to give an ivory colored solid. The crude amino-phosphine was dissolved in MeOH (20 ml) to give a pale yellow solution. To the solution of amino-phosphine was added sequentially hydroxylamine HCl salt (1.4 g, 20.0 mmol) followed by fresh solid NaOMe powder (1.3 g, 24.0 mmol) to make a milky pH 10 suspension. After 36 h, the reaction was complete by LCMS. The reaction was evaporated under reduced pressure to give a yellow solid that was dried in vacuo. The crude product (2.75 g) was triturated with ether (3×50 ml) to remove impurities (P(O)Ph₃) and then was dissolved in abs. EtOH (120 ml) with sonication for 15 min. A fine white powder was suction filtered off, and the clear yellow ethanolic portion was concentrated to a small volume. The crude product was dissolved in DMSO (8 ml) and purified by preparative HPLC (Ultro 120 C18 75×300 mm column) running a gradient (AcCN/water, 0.1% TFA) from 5 to 70% for 55 min. The purified fractions were pooled together and lyophilized to dryness. The product as the TFA salt was dissolved in AcCN/water (50:50) (100 ml), 1N aq. HCl (1 equivalent) and lyophilized again to give 325 mg of light yellow powder as the HCl salt (43% yield).

HPLC (220 nm, 41 min.run) 18.31 min.; HPLC (220 nm, 17 min.run) 9.11 min; LCMS: LC (214 nm) 1.91 min., MS (ES+) m/z 338.1 (C₁₉H₁₉N₃O₃+H requires 338.14).

Synthesis of 4′-(N-Acylamino)-Tolan Dap Analogs Example 14 Synthesis of 4-({4-[(aminoacetyl)amino]phenyl}ethynyl)-N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2-oxoethyl]benzamide

Preparation of 2-N-Boc-amino-N-(4-iodo-phenyl)-acetamide (2)

Reagent MW Eq. g/ml mmol Boc-Gly-OH 175.19 1.00 1.752 g 10.0 4-Iodoaniline (1) 219.03 1.04 2.290 g 10.4 EDCI 191.71 1.04 1.994 g 10.4 HOBt 135.13 1.00 1.351 g 10.0 DCM 18 mL DMF 1 mL

A solution of Boc-Gly-OH (1.752 g, 10.0 mmol) in DCM (18 mL) and DMF (1 mL) was treated with EDCI (1.994 g, 10.4 mmol) and HOBt (1.351 g, 10.0 mmol). After stirring 15 min, 4-iodoaniline 1 (2.290 g, 10.4 mmol) was added and the reaction monitored by TLC (25:1 DCM/MeOH(R_(f)=0.6)). After 24 h the solution was diluted with EtOAc (250 mL), washed with 1.0 M HCl (3×100 mL), sat. NaHCO₃ (3×100 mL), brine (3×100 mL), dried over MgSO₄, filtered and concentrated in vacuo to afford 2.900 g (77% yield) of a white solid.

Preparation of (2S)-3-N-Boc-amino-(4-ethynyl-benzoylamino)-propionic acid methyl ester (4)

Reagent MW Eq. g/mL mmol 4-Ethynylbenzoic acid (3) 146.14 1.0 0.910 g 6.22 H-Dap(Boc)-OMe-HCl 254.71 1.2 1.903 g 7.47 EDCI 191.71 1.2 1.432 g 7.47 HOBt 135.13 1.1 0.910 g 6.73 DIEA 129.25 3.2 3.5 mL 20.0 DMF 50 mL

Triethylamine (3.5 mL, 20.0 mmol) was added to a stirred solution of 4-ethynylbenzoic acid 3 (910 mg, 6.22 mmol), H-Dap(Boc)-OMe hydrochloride (1.903 g, 7.47 mmol), EDCI (1.432 g, 7.47 mmol), and HOBt (910 mg, 6.73 mmol) in DMF (50.0 mL). After stirring 20 h, the reaction mixture was diluted with EtOAc (400 mL), washed with 1.0 M HCl (2×100 mL), saturated NaHCO₃ (2×100 mL), H₂O (4×100 mL), dried over MgSO₄, filtered and concentrated in vacuo to give 2.140 g (99% yield) of a tan solid, mp=110-111° C. LRMS (ES+) m/z 346.9 (C₁₈H₂₂N₂O₅+H requires 347.10).

To a suspension of methyl (2S)-3-[(tert-butoxy)carbonylamino]-2-[(4-ethynylphenyl)carbonylamino]propanoate (4) (200 mg, 0.577 mmol) and 2-[(tert-butoxy)carbonylamino]-N-(4-iodophenyl)acetamide (2) (476 mg, 1.26 mmol) was added Et₃N (350 μL, 2.5 mmol). The solution was purged with a stream of N₂ for several minutes and PdCl₂(PPh₃)₂ (20 mg, 0.028 mmol) and CuI (10.6 mg, 0.055 mmol) were added. The reaction mixture was stirred at ambient temperature for 22 h and then concentrated by rotary evaporation. The crude black residue was chromatographed twice by silica gel chromatography (30:1 CH₂Cl₂/MeOH) to give 285 mg (83%) of methyl (2S)-3-[(tert-butoxy)carbonylamino]-2-({4-[2-(4-{2-[(tert-butoxy)carbonylamino]acetylamino}phenyl)ethynyl]phenyl}carbonylamino) propanoate (5) as a yellow foam.

To a solution of hydroxylamine hydrochloride (98 mg, 1.41 mmol) in MeOH (1.3 mL) at 0° C. was added 25 wt % NaOMe (460 mg, 2.13 mmol). The solution was stirred at 0° C. for 15 min and then charged with a solution of methyl (2S)-3-[(tert-butoxy)carbonylamino]-2-({4-[2-(4-{2-[(tert-butoxy)carbonylamino]acetylamino}phenyl)ethynyl]phenyl}carbonylamino)propanoate (4) (279 mg, 0.469 mmol) in THF (1.5 mL) and MeOH (0.6 mL). The reaction was stirred at 0° C. for 30 min and at room temperature for 2.5 h. The reaction mixture was diluted with 4:1 CHCl₃/iPrOH (50 ml) and washed with 0.1 M HCl (30 mL). The layers were separated and the aqueous layer extracted once more with 4:1 CHCl₃/iPrOH (30 ml). The organic layers were combined, dried over Na₂SO₄, filtered and concentrated. The crude residue was suspended in 10:1 CH₂Cl₂/MeOH (4 mL), filtered, and washed with 50:1 CH₂Cl₂/MeOH (2 mL) and Et₂O (10 mL) to afford 180 mg (64%) of N-(4-{2-[4-(N-{1-(N-hydroxycarbamoyl)(1S)-2-[(tert-butoxy)carbonylamino]ethyl}carbamoyl)phenyl]ethynyl}phenyl)-2-[(tert-butoxy)carbonylamino]acetamide (6) as a white powder.

To an oven-dried flask containing N-(4-{2-[4-(N-{1-(N-hydroxycarbamoyl)(1S)-2-[(tert-butoxy)carbonylamino]ethyl}carbamoyl)phenyl]ethynyl}phenyl)-2-[(tert-butoxy)carbonylamino]acetamide (6) (130 mg, 0.218 mmol) was added 1:1 TFA/CH₂Cl₂ (2.5 mL). The resulting pink solution was stirred for 2 h and concentrated to give a pink gum. The crude residue was rinsed with CH₂Cl₂ (4 mL), concentrated by rotary evaporation and dissolved in THF (2 mL) and MeOH (0.4 mL). A solution of 4 M HCl in dioxane (200 μL) was added and the resulting precipitate filtered and washed with Et₂O (10 mL) to afford 90 mg of 4-({4-[(aminoacetyl)amino]phenyl}ethynyl)-N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2-oxoethyl]benzamide as a pale tan powder.

Reaction of Iodoaniline with Bromoacetyl Bromide

Bromoacetyl bromide (175 mL, 2.00 mmol) was added dropwise over 5 minutes to a solution of 4-iodoaniline (438 mg, 2.00 mmol) and Et₃N (280 μL, 2.00 mmol) in benzene (5 mL). The reaction was stirred 1 hour, treated with morpholine (1.0 mL, 11.5 mmol) and stirred overnight. The reaction mixture was diluted with EtOAc (200 mL), washed with aqueous 0.1 M KOH (50 mL), H₂O (50 mL), dried over MgSO₄ and concentrated to give a yellow oil. Purification by silica gel chromatography (100:1 CH₂Cl₂/MeOH) afforded 630 mg (91%) of N-(4-iodophenyl)-2-morpholin-4-ylacetamide as a waxy tan solid. This product was converted to analogues in a similar manner as Example 14.

Example A Preparation of 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid methyl ester

Reagent MW EQ g/ml mmol H-DAP(Boc)-OMe (1) 254 1.05 5.93 g 23.3 4-Iodo-benzoic acid 248 1.0 5.49 g 22.2 HOAT 136.1 1.02 3.08 g 22.6 EDC 191.71 1.02 4.33 g 22.6 DIEA 129.25 2.5 9.7 ml 55.1 DMF 85 ml

DIEA (9.7 ml, 55.1 mmol) was added to a stirred solution of 4-iodo-benzoic acid (5.49 g, 22.2 mmol), HOAT (3.08 g, 22.6 mmol), EDC (4.33 g, 22.6 mmol) in DMF (85 ml). After 2 min., the H-DAP(Boc)-OMe (1) was added in one portion. After 12 hours, the reaction was found complete by LCMS. The reaction was diluted with EtOAc/hexane (1:1) (500 ml). The organic phase was washed with 1N HCl (2×80 ml), 1N NaOH (2×80 ml), water (2×80 ml), sat. brine (80 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The residue was filtered through a filter plug of silica eluting with EtOAc/hexane (1:1). The fractions with product were evaporated to give 9.3 g of product (3-tert-Butoxycarbonylamino-2-(4-iodo-benzoylamino)-propionic acid methyl ester) in 93% yield. This product was converted to analogues in a similar manner as the aforementioned Examples.

Example 15 N-(1-(N-hydroxycarbamoyl)(1S,2R)-2-hydroxypropyl)(4-{2-[4-(morpholin-4-ylmethyl)phenyl]ethynyl}phenyl)carboxamide (5)

Preparation of (2S,3R)-2-[4-(4-formyl-phenylethynyl)-benzoylamino]-3-hydroxy-butyric acid methyl ester (3)

Reagent MW Eq. g/ml mmol Ethynylbenzene (1) 261.27 1.0 0.745 g 2.85 4-Iodobenzaldehyde (2) 232.00 1.4 0.902 g 3.89 PdCl₂(PPh₃)₂ 701.89 0.03 0.070 g 0.10 CuI 190.44 0.06 0.034 g 0.18 Et₃N 101.19 2.3 0.90 mL 6.5 THF 50 mL

A solution of alkyne 1 (745 mg, 2.85 mmol), 4-iodobenzaldehyde 2 (902 mg, 3.89 mmol), and Et₃N (900 μL, 6.5 mmol) in THF (50 mL) was purged with a stream of N₂ for two minutes and then treated with PdCl₂(PPh₃)₂ (70 mg, 0.10 mmol) and CuI (34 mg, 0.18 mmol). The reaction mixture was stirred 40 h, concentrated by rotary evaporation and purified by silica gel chromatography (40:1 DCM/MeOH) to give 0.833 g (80% yield) of (2S,3R)-2-[4-(4-formyl-phenylethynyl)-benzoylamino]-3-hydroxy-butyric acid methyl ester 3 as a pale yellow powder, mp=143-144° C. R_(f)=0.3 (25:1 DCM/MeOH); LRMS (ES+) m/z 366.1 (C₂₁H₁₉NO₅+H requires 366.13); HPLC (300 nm, 47 min) 15.3 min.

Preparation of (2S,3R)-3-Hydroxy-2-[4-(4-morpholin-4-ylmethyl-phenylethynyl)-benzoylamino]-butyric acid methyl ester (4)

Reagent MW Eq. g/ml mmol Tolanylaldehyde (3) 365.38 1.0 0.822 g 2.25 Morpholine 87.12 1.3 0.260 mL 2.97 NaBH(OAc)₃ 211.94 1.4 0.670 g 3.16 THF 15 ml

Sodium triacetoxyborohydride (0.670 g, 3.16 mmol) was added to a solution of benzaldehyde 3 (0.822 g, 2.25 mmol) and morpholine (260 μL, 2.97 mmol) in THF (15 mL) under N₂ atmosphere and the reaction monitored by TLC (25:1 DCM/MeOH, R_(f)=0.2). After stirring 4 h, the reaction mixture was quenched with saturated NaHCO₃ (150 mL), extracted with EtOAc (3×100 mL), dried over MgSO₄, filtered and concentrated to give a yellow syrup. Purification by silica gel chromatography (35:1 DCM/MeOH) afforded 0.844 g (86% yield) of 4 as a sticky white foam.

Preparation of (2S,3R)—N-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-(4-morpholin-4-ylmethyl-phenylethynyl)-benzamide (5)

Reagent MW Eq. g/ml mmol Methyl ester (4) 436.50 1.0 0.829 g 1.90 NH₂OH—HCl 69.49 3.0 0.400 g 5.76 NaOMe (25 wt %) 54.02 4.5 1.860 g 8.60 MeOH 8 mL THF 3 mL

Sodium methoxide (25 wt % in MeOH, 1.860 g, 8.60 mmol) was added to a stirred solution of hydroxylamine hydrochloride (400 mg, 5.76 mmol) in anhydrous MeOH (5 mL) at 0° C. under N₂ atmosphere. After stirring 20 min, a solution of methyl ester 4 (829 mg, 1.90 mmol) in 1:1 MeOH/THF (6 mL) was added and the reaction mixture stirred at 0° C. for 1 h and at room temperature for 4 h. The reaction was quenched with 1.0 M HCl (6 mL), concentrated by rotary evaporation to remove organic solvents, and diluted with DMSO (4 mL). Analytical RP-HPLC (C₁₈ column, CH₃CN gradient 5-35%, 0.1% TFA, UV analysis 300 nm, 16 min) indicated a purity of 85% for the crude product mixture. Purification by preparative RP-HPLC and lyophilization of the collected fractions gave 701 mg (81%) of 5 as a fluffy white solid. LRMS (ES+) m/z 438.1 (C₂₄H₂₇N₃O₅+H requires 438.20); RP-HPLC (300 nm, 16 min run) 8.7 min.

Resin Procedures for Synthesizing Tolanyl hydroxamates

Example 16 Synthesis of 4-[(4-{[(benzylamino)acetyl]amino}phenyl)ethynyl]-N-{(1S,2R)-2-hydroxy-1-[(hydroxyamino)carbonyl]propyl}benzamide

1. Coupling to Fmoc Hydroxylamine Resin

The resin was pre-swelled by adding DCM and shaking for 30 min. The resin was drained, 20% piperidine was added in DMF, the resin was shaken 1.25 hours, and finally drained and washed in 2×DMF and 2×DCM. After draining completely, 20% piperidine in DMF was added to attain cleavage in 1.25 hours. The resin was washed 4×DMF, 4×DCM and drained completely. In a separate flask, the amino acid (Fmoc-Thr tBu-OH, or Fmoc-DAP Boc-OH, 4 eq) was mixed, HATU (4 eq), DMF (60 ml) and Hunig's (8 eq) base were added and stirred for 2-3 min. The mixture was added to the resin and shaken 20-24 hours. Subsequently, the resin was drained and run with a standard wash (1×DCM, 4×DMF and 4×DCM). The Fmoc was removed from the amino acid by adding 20% piperidine in DMF and shaken 1.25 hours, drained, and given the standard wash (1×DCM, 4×DMF and 4×DCM).

2. Coupling of 4-Iodobenzoic Acid to Amino Acid Resin

A mixture of 4-iodobenzoic acid (4 eq), HBTU (4 eq), DMF (60 ml) was shaken for several minutes. Hünig's base (8 eq) was subsequently added and the mixture was shaken further for 2-3 min. The pre-activated mixture was then added to the prepared Thr or DAP resin (Fmoc removed, 7.5 g, 5.775 mmol). The reaction is shaken 12-16 hours followed by the standard wash (1×DCM, 4×DMF and 4×DCM).

3. Alkyne Coupling on Resin

To the 4-iodobenzoic resin (4 g, 3.08 mmol) was added 4-aminophenylacetylene (3 eq), Pd(PPh₃)₂Cl₂ (0.04 eq), CuI (0.08 eq) and THF (purged with Argon). After mixing for 1 min., TEA (4.5 eq) was added and the reaction was shaken 12 hours at RT under argon.

4. Aniline Coupling with Bromoacetyl Chloride on Resin

To aniline resin (4 g, 3.08 mmol) was added DCM (30 ml) lutidine (10 eq) and shaken for 1 min. Bromoacetyl chloride (8 eq) in DCM (5 ml) was added slowly. After the addition, the slurry was shaken for 1.5 to 1.75 hours. Subsequent draining and a wash with 2×DCM, 4×DMF and 4×DCM was then performed.

5. Displacement with Amines on Resin

To the bromoacetyl resin (125 mg), was added NMP (1.5 ml) followed by amine (0.2 g or m1, ie excess) and the slurry was shaken for 12-16 hours at RT. To neutralize the salt, TEA was added. The imidazole was heated at 38° C. for 24 h (in the case of anilines, they were heated at 38° C. for 48 h). The reaction mixture was drained and washed 4×DMF and 4×DCM.

6. Cleavage from Resin and Deprotection of Thr tBu and DAP Boc

The resin (125 mg) was soaked in TFA/water (80:20 v/v) (1.5 ml) at RT for 45 min. Upon cleavage the solution was collected and the resin was washed with more TFA/water mixture (0.75 ml). To the TFA/product solution was added acetonitrile/water solution (1:1 v/v, 10 ml) and pure water (2.5 ml). The mixture was frozen in liquid nitrogen for 15 min and lyophilized. The dry residue was dissolved in the acetonitrile/water solution (1:1 v/v, 10 ml) again followed by addition of 1M aq. HCl (1.2 eq per basic nitrogen), frozen, and lyophilized to a powder.

Synthesis of 3′-Nitro-Tolan Threonine Hydroxamic Acid Example 17 (1S,2R)—N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-4-(3-nitro-phenylethynyl)-benzamide

Preparation of (1S,2R)—N-(2-tert-butoxy-1-hydroxycarbamoyl-propyl)-4-ethynyl-benzamide on hydroxylamine 2-chlorotrityl resin (3)

Reagent MW Eq. g/mL mmol Fmoc-threonine/resin (1) 0.70 mmol/g 1.0 0.522 g 0.365 4-Ethynylbenzoic acid (2) 146.14 3.0 0.160 g 1.10 DIC 126.20 4.9 0.28 mL 1.79 HOBt 135.13 3.0 0.148 g 1.10 DIEA 129.25 6.3 0.40 mL 2.30 DCM 1.0 mL DMF 3.0 mL

The resin 1 (0.522 g, 0.365 mmol, 0.70 mmol/g) was swelled in DCM (5 mL) for 2 h and drained. The resin was treated with 20% piperidine in DMF (6 mL) for 1 hour, washed with DMF (4×6 mL) and DCM (4×6 mL) and drained completely. In a separate flask, 4-ethynylbenzoic acid 2 (0.160 g, 1.10 mmol), DIC (0.280 mL, 1.79 mmol), HOBt (0.148 g, 1.10 mmol) and DIEA (0.4 mL, 2.30 mmol) were dissolved in DCM (1 mL) and DMF (4 mL), stirred 15 min and added to the resin. After shaking for 36 h, the mixture was drained, washed with DMF (4×6 mL) and DCM (4×6 mL) and dried in vacuo to give 0.495 g of a yellow resin.

Preparation of (1S,2R)—N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-4-(3-nitro-phenylethynyl)-benzamide (5)

Reagent MW Eq. g/mL mmol Alkyne on resin (3) 0.70 mmol/g 1.0 100 mg 0.070 1-Iodo-3-nitrobenzene (4) 249.01 5.0 87.1 mg 0.350 PdCl₂(PPh₃)₂ 701.89 0.2 10.0 mg 0.014 CuI 190.44 0.5 7.0 mg 0.036 Et₃N 101.19 15 150 μL 1.10 DMF 1.5 mL

Resin 3 (100 mg, 0.070 mmol) was swelled in DCM (2 mL) for 1 h and drained. A solution of 1-iodo-3-nitrobenzene 4 (87.1 mg, 0.350 mmol) and Et₃N (150 μL, 1.10 mmol) in DMF (1.5 mL) was purged with a stream of N₂ bubbles for two minutes and added to the resin. After mixing for 5 min, PdCl₂(PPh₃)₂ (10.0 mg, 0.014 mmol) and CuI (7.0 mg, 0.036 mmol) were added and the mixture shaken for 26 h. The resin was drained, washed with DMF (3×2 mL), DCM (3×2 mL) and cleaved with 10% TFA/DCM (1.5 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (1.0 mL). The cleavage fractions were combined, treated with neat TFA (2.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-65%, 0.1% TFA, UV analysis 300 nm, 28 min) and lyophilization of the collected fractions afforded 6.0 mg (22% yield) of (1S,2R)—N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-4-(3-nitro-phenylethynyl)-benzamide as a white foam. LRMS (ES+) m/z 384.2 (C₁₉H₁₇N₃O₆+H requires 384.15); RP-HPLC (300 nm, 28 min run) 15.2 min.

Synthesis of 4′-Trifluoromethoxy-Tolan Dap Hydroxamic Acid Example 18 (1S)—N-(2-amino-1-hydroxycarbamoyl-ethyl)-4-(4-trifluoromethoxy-phenylethynyl)-benzamide (5)

Preparation of (1S)—N-(2-(Boc)-amino-1-hydroxycarbamoyl-ethyl)-4-ethynyl-benz-amide on hydroxylamine 2-chlorotrityl resin (3)

Reagent MW Eq. g/mL mmol Fmoc-Dap/resin (1) 0.70 mmol/g 1.0 1.330 g 0.931 4-Ethynylbenzoic acid (2) 146.14 3.0 0.408 g 2.793 DIC 126.20 4.8 0.70 mL 4.470 HOBt 135.13 3.0 0.377 g 2.793 DIEA 129.25 6.2 1.0 mL 5.7 DCM 10.0 mL DMF 2.0 mL

The resin 1 (1.330 g, 0.931 mmol, 0.70 mmol/g) was swelled in DCM (15 mL) for 2 h and drained. The resin was treated with 20% piperidine in DMF (20 mL) for 1 hour, washed with DMF (3×15 mL) and DCM (3×15 mL) and drained completely. In a separate flask, 4-ethynylbenzoic acid 2 (0.408 g, 2.793 mmol), DIC (0.70 mL, 4.470 mmol), HOBt (0.377 g, 2.793 mmol) and DIEA (1.0 mL, 5.7 mmol) were dissolved in DCM (10 mL) and DMF (2 mL), stirred 15 min and added to the resin. After shaking for 36 h, the mixture was drained, washed with DMF (3×15 mL) and DCM (3×15 mL) and dried in vacuo to give 1.290 g of a yellow resin.

Preparation of (1S)—N-(2-amino-1-hydroxycarbamoyl-ethyl)-4-(4-trifluoromethoxy-phenylethynyl)-benzamide (5)

Reagent MW Eq. g/mL mmol Alkyne on resin (3) 0.70 mmol/g 1.0 120 mg 0.084 4-CF₃O-iodobenzene (4) 287.99 4.0 96.8 mg 0.336 PdCl₂(PPh₃)₂ 701.89 0.3 18.0 mg 0.025 CuI 190.44 0.5 8.0 mg 0.042 Et₃N 101.19 13 150 μL 1.10 DMF 2.0 mL

Resin 3 (120 mg, 0.084 mmol) was swelled in DCM (2 mL) for 1 h and drained. A solution of 4-(trifluoromethoxy)iodobenzene 4 (96.8 mg, 0.336 mmol) and Et₃N (150 μL, 1.10 mmol) in DMF (2.0 mL) was purged with a stream of N₂ bubbles for two minutes and added to the resin. After mixing for 5 min, PdCl₂(PPh₃)₂ (18.0 mg, 0.025 mmol) and CuI (8.0 mg, 0.042 mmol) were added and the mixture shaken for 24 h. The resin was drained, washed with DMF (3×2 mL), DCM (3×2 mL) and cleaved with 10% TFA/DCM (2.0 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (1.0 mL). The cleavage fractions were combined, treated with neat TFA (3.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-55%, 0.1% TFA, UV analysis 300 nm, 28 min) and lyophilization of the collected fractions afforded 9.0 mg (25% yield) of (1S)—N-(2-amino-1-hydroxycarbamoyl-ethyl)-4-(4-trifluoromethoxy-phenylethynyl)-benzamide as a white solid. LRMS (ES+) m/z 408.0 (C₁₉H₁₆F₃N₃O₄+H requires 408.11); RP-HPLC (300 nm, 28 min run) 18.0 min.

Example 19 Synthesis of N-(1-(N-hydroxycarbamoyl)(1S,2R)-2-hydroxypropyl)[4-(4-phenylbuta-1,3-diynyl)phenyl]carboxamide

Reagent MW EQ g/ml mmol Dibromovinylbenzoic acid (2) 320 1.0 5.76 g 18.0 Ethynyl-benzene 102 1.4 2.57 g 25.2 Pd₂dba₃ 915 0.01 164 mg 0.18 (1% cat.) TMPP 352 0.04 253 mg 0.72 (4%) TEA 101 3.0 7.5 ml 54.0 DMF 60 ml degassed with argon The 4-(2,2-Dibromo-vinyl)-benzoic acid methyl ester (2) was made by the method of Wang Shen and Le Wang in J. Org. Chem. 1999, 64, 8873-8879.

A solution of 4-(2,2-dibromo-vinyl)-benzoic acid methyl ester (2) (5.76 g, 18.0 mmol), ethynyl-benzene (2.57 g, 25.2 mmol), Pd₂ dba₃ (164 mg, 0.18 mmol), tris(4-methoxyphenyl) phosphine (TMPP) (253 mg, 0.72 mmol) were dissolved in argon sparged (5 min.) DMF (60 ml). The reaction was sparged with argon for 1 min. TEA (7.5 ml, 54.0 mmol) was added to the stirred reaction mixture that was then heated under argon at 85° C. for 3.5 hours. The reaction was found complete by LCMS. The reaction was cooled to rt and diluted with EtOAc/hexane (1:1) (300 ml). The organic phase was washed with 1M HCl (2×50 ml), 1M NaOH (3×50 ml), water (2×50 ml), sat. brine (50 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure to obtain 5.25 g of crude product as an oil. The oil was treated with approximately 20 ml of a solution of 20% EtOAc/hexane that was heated to dissolve the residue. The walls of the flask were washed with the 20% EtOAc/hexane solution (5 ml) that upon cooling gave 1.45 g of pure product (31% yield) as a white solid. The balance of the crude reaction product was purified by flash chromatography using EtOAc (8%)/hexane as eluant. The pure fractions were evaporated and dried in vacuo to give addition product typically 25-30% addition yield.

4-(4-Phenyl-buta-1,3-diynyl)-benzoic acid methyl ester (4) was made according to the method of Wang Shen and Sheela A. Thomas in Org. Lett. 2000, 2(18), 2857-2860.

Preparation of 4-(4-Phenyl-buta-1,3-diynyl)-benzoic acid (5)

A 3M aq. solution of NaOH (20 ml) was added to a stirred solution of methyl ester 4 (1.45 g, 5.6 mmol) in MeOH (100 ml) at rt. The reaction solution was heated to reflux for 45 min. until the reaction turned clear. All of the starting material was gone by TLC and HPLC. The reaction was cooled to rt and some MeOH (˜50 ml) was removed by evaporation under reduced pressure. Water (100 ml) was added to the mixture. Conc. HCl was added dropwise to the stirred solution until acidic by pH paper (pH2). The white precipitate that formed was collected by suction filtration. The solid was washed with water (3×20 ml) and hexane (2×20 ml) to give after drying 1.35 g of product acid 5 in 99% yield.

Subsequent conversion of compound 5 to compound 7 was performed according to the method described in Example 12 for the synthesis of N-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-phenylethynyl-benzamide (compound 5). LCMS MH+ 363.13.

Example B Synthesis of N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2-oxoethyl]-4-[4-(4-aminophenyl)buta-1,3-diynyl]benzamide Preparation of 2-{4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-benzoylamino}-3-tert-butoxycarbonylamino-propionic acid methyl ester (2)

Reagent MW EQ g/ml mmol H-DAP(Boc)-OMe 254 1.05 5.12 g 20.1 1,3-diynyl benzoic acid (1) 261.3 1.0 5.0 g 19.1 HOBT 135.1 1.05 2.72 g 20.1 EDC 191.71 1.05 3.85 g 20.1 DIEA 129.25 3.0 10.5 ml 60.3 DMF 80 ml

DIEA (10.5 ml, 60.3 mmol) was added to a stirred solution of 4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-benzoic acid (1) (5.0 g, 19.1 mmol), HOBT (2.72 g, 20.1 mmol), EDC (3.85 g, 20.1 mmol) in DMF (80 ml). After 2 min., the H-DAP(Boc)-OMe was added in one portion. After 12 hours at rt, the reaction was found complete by LCMS. The reaction was diluted with EtOAc/hexane (4:1) (500 ml). The organic phase was washed with 1N NaOH (2×80 ml), water (2×80 ml), sat. brine (80 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The residue was filtered through a filter plug of silica eluting with EtOAc/hexane (4:1). The fractions with product were evaporated to give 8.02 g of product in 91% yield.

Subsequent conversion of compound 2 to the final hydroxamic acid (for example, Example 892) was performed according to the method described in Example 12 for the synthesis of N-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-phenylethynyl-benzamide (compound 5).

Synthesis of 4-(Buta-1,3-diynyl)-benzoic Acid (4) for making 1,3-diynyl analogues (such as Example 20 below)

Preparation of 4-(4-trimethylsilanyl-buta-1,3-diynyl)-benzoic acid methyl ester (3)

Reagent MW Eq. g/ml mmol Methyl 4-iodobenzoate (2) 262.04 1.0 4.510 g 17.2 Trimethylsilylbutadiyne (1) 122.24 2.5 5.240 g 42.8 PdCl₂(PPh₃)₂ 701.89 0.04 0.483 g 0.690 CuI 190.44 0.08 0.262 g 1.37 Et₃N 101.19 3.0 7.2 mL 52.0 CH₃CN 50 mL

A solution of methyl 4-iodobenzoate 2 (4.510 g, 17.2 mmol), PdCl₂(PPh₃)₂ (483 mg, 0.690 mmol), and CuI (262 mg, 1.37 mmol) in CH₃CN (50 mL) was cooled to 0° C. under N₂ atmosphere in the absence of light. Triethylamine (7.2 mL, 52.0 mmol) was added, followed by trimethylsilyl-1,3-butadiyne 1 (5.240 g, 42.8 mmol) and the reaction stirred 3 h at 0° C. and 30 h at ambient temperature. Removal of solvent by rotary evaporation afforded a crude black residue that was purified by silica gel chromatography (95:5 hexanes/EtOAc) to give 3.450 g (79% yield) of 4-(4-trimethylsilanyl-buta-1,3-diynyl)-benzoic acid methyl ester 3 as a brown solid, mp=67-68° C.

Preparation of 4-(buta-1,3-diynyl)-benzoic acid (4)

Reagent MW Eq. g/ml mmol Methyl ester (3) 252.34 1.0 3.420 g 13.5 KOH 56.11 4.9 3.700 g 65.9 H₂O 10 mL THF 26 mL

Potassium hydroxide (3.700 g, 65.9 mmol) was dissolved in H₂O (10 mL) and added to a solution of 4-(4-trimethylsilanyl-buta-1,3-diynyl)-benzoic acid methyl ester 3 (3.420 g, 13.5 mmol) in THF (26 mL) in the absence of light. After stirring 16 h, the reaction was quenched with 1.0 M HCl (120 mL) and the resulting precipitate was filtered, washed with 1:1 hexanes/benzene (150 mL) and dried in vacuo to afford 2.100 g (91% yield, 98% pure) of 4-(buta-1,3-diynyl)-benzoic acid 4 as a brown solid, mp >230° C. Although diyne 4 was found to be unstable at room temperature it could be stored for several weeks at 0° C. with only small amounts of decomposition observed by TLC. R_(f)=0.2 (4:1 Hexanes/EtOAc); HPLC (300 nm, 28 min run) 16.0 min; LRMS (ES+) m/z 171.0 (C₁₁H₆O₂+H requires 171.04).

Synthesis of a 3′-Nitrophenyl-Diacetylenic-Dap Hydroxamic Acid Example 20 N-(1-(N-hydroxycarbamoyl)(1S)-2-aminoethyl) {4-[4-(3-nitrophenyl)buta-1,3-diynyl]phenyl}carboxamide (6)

Preparation of Fmoc-Dap(Boc)-NHOH on hydroxylamine 2-chlorotrityl resin (2)

Reagent MW Eq. g/mL mmol Hydroxylamine resin (1) 0.77 mmol/g 1.0 3.288 g 2.53 Fmoc-Dap(Boc)-OH 426.47 3.0 3.175 g 7.44 HATU 380.25 3.0 2.829 g 7.44 DIEA 129.25 10.0 4.3 mL 24.7 DMF 35 mL

A suspension of N-Fmoc-hydroxylamine 2-chlorotrityl resin (3.288 g, 2.53 mmol, 0.77 mmol/g, Novabiochem) in DCM (40 mL) was shaken for 2 h and drained. The resin was treated with 20% piperidine in DMF (40 mL) for 1 hour, washed with DMF (2×40 mL), treated a second time with 20% piperidine in DMF (40 mL), washed with DMF (3×40 mL) and DCM (3×40 mL) and drained completely. In a separate flask, Fmoc-Dap(Boc)-OH (3.175 g, 7.44 mmol), HATU (2.829 g, 7.44 mmol) and DIEA (4.3 mL, 24.7 mmol) were dissolved in DMF (35 mL), stirred three minutes and added to the resin. After shaking for 48 h, the mixture was drained, washed with DMF (4×40 mL) and DCM (4×40 mL) and dried in vacuo to give 3.530 g of a yellow resin.

Preparation of (S)—N-(2-N-Fmoc-amino-1-hydroxycarbamoyl-ethyl)-4-buta-1,3-diynyl-benzamide on hydroxylamine 2-chlorotrityl resin (4)

Reagent MW Eq. g/mL mmol Fmoc-Dap(Boc)/resin (2) 0.71 mmol/g 1.0 3.530 g 2.53 Butadiynyl benzoic acid (3) 170.16 2.5 1.076 g 6.32 EDCI 191.71 3.0 1.457 g 7.60 HOBt 135.13 3.0 1.048 g 7.75 DIEA 129.25 5.0 2.2 mL 12.6 DCM 25 mL DMF 5 mL

The resin 2 (3.530 g, 2.53 mmol, 0.71 mmol/g) was swelled in DCM (40 mL) for 2 h and drained. The resin was treated with 20% piperidine in DMF (40 mL) for 1 hour, washed with DMF (4×40 mL) and DCM (4×40 mL) and drained completely. In a separate flask, 4-buta-1,3-diynyl-benzoic acid 3 (1.076 g, 6.32 mmol), EDCI (1.457 g, 7.60 mmol), HOBt (1.048 g, 7.75 mmol) and DIEA (2.2 mL, 12.6 mmol) were dissolved in DCM (25 mL) and DMF (5 mL), stirred 45 min and added to the resin. After shaking for 48 h, the mixture was drained, washed with DMF (4×40 mL) and DCM (4×40 mL) and dried in vacuo to give 3.35 g of a pale brown resin.

Preparation of (S)—N-(2-amino-1-hydroxycarbamoyl-ethyl)-4-[4-(3-nitro-phenyl)-buta-1,3-diynyl]-benzamide (6)

Reagent MW Eq. g/mL mmol Diacetylene on resin (4) 0.77 mmol/g 1.0 176 mg 0.135 1-Iodo-3-nitrobenzene (5) 249.01 3.5 118 mg 0.474 PdCl₂(PPh₃)₂ 701.89 0.07 6.0 mg 0.009 CuI 190.44 0.38 10.0 mg 0.052 Et₃N 101.19 10.6 200 μL 1.43 DMF 3.0 mL

Resin 4 (176 mg, 0.135 mmol) was swelled in DCM (3 mL) for 1 h and drained. A solution of 1-iodo-3-nitrobenzene 5 (118 mg, 0.474 mmol) and Et₃N (200 μL, 1.43 mmol) in DMF (3.0 mL) was purged with a stream of N₂ bubbles for two minutes and added to the resin. After mixing for 5 min, PdCl₂(PPh₃)₂ (6.0 mg, 0.009 mmol) and CuI (10.0 mg, 0.052 mmol) were added and the mixture shaken for 36 h. The resin was drained, washed with DMF (4×3 mL), DCM (4×3 mL) and cleaved with 10% TFA/DCM (2 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (2 mL). The cleavage fractions were combined, treated with neat TFA (4.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-65%, 0.1% TFA, UV analysis 300 nm, 30 min) and lyophilization of the collected fractions afforded 12.0 mg (22%) of 470 as a white solid. LRMS (ES+) m/z 392.9 (C₂₀H₁₆N₄O₅+H requires 393.11); RP-HPLC (300 nm, 30 min run) 14.9 min.

Synthesis of 4′-Benzamide Diacetylene Dap Hydroxamic Acid Example 21 N-((2S)-amino-1-hydroxycarbamoyl-ethyl)-4-{4-[4-(2-amino-ethylcarbamoyl)-phenyl]-buta-1,3-diynyl}-benzamide (3)

Preparation of N-((2S)-amino-1-hydroxycarbamoyl-ethyl)-4-{4-[4-(2-amino-ethylcarbamoyl)-phenyl]-buta-1,3-diynyl}-benzamide (3)

Reagent MW Eq. g/mL mmol Alkyne on resin (1) 0.77 mmol/g 1.0 145 mg 0.111 4-Ethynylbenzamide (2) 430.54 2.6 124 mg 0.288 PdCl₂(PPh₃)₂ 701.89 0.3 21 mg 0.030 CuI 190.44 1.0 22 mg 0.110 Et₃N 101.19 6.5 100 μL 0.72 DMF 2.0 mL

Resin 1 (145 mg, 0.111 mmol) was swelled in DCM (2 mL) for 1 h and drained. A solution of 4-ethynylbenzamide 2 (124 mg, 0.288 mmol) and Et₃N (100 μL, 0.72 mmol) in DMF (2.0 mL) was added and the resin agitated for 5 min. A mixture of PdCl₂(PPh₃)₂ (21 mg, 0.030 mmol) and CuI (22 mg, 0.110 mmol) was added and the resin was agitated for 60 h. The resin was drained, washed with DMF (3×2 mL), DCM (3×2 mL) and cleaved with 10% TFA/DCM (1.5 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (1.0 mL). The cleavage fractions were combined, treated with neat TFA (2.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-55%, 0.1% TFA, UV analysis 300 nm, 26 min) and lyophilization of the collected fractions afforded 2.6 mg (5% yield) of N-((2S)-amino-1-hydroxycarbamoyl-ethyl)-4-{4-[4-(2-amino-ethylcarbamoyl)-phenyl]-buta-1,3-diynyl}-benzamide. LRMS (ES+) m/z 434.0 (C₂₃H₂₃N₅O₄+H requires 434.19); RP-HPLC (300 nm, 26 min run) 15.3 min.

Synthesis of N-[4-Butadiynyl-benzoyl]-Thr(tBu) on Resin (Continued to make Examples 22 and 23)

Preparation of (2S,3R)-2-N-Fmoc-amino-3-tert-butoxy-N-hydroxy-butyramide on hydroxylamine 2-chlorotrityl resin (2)

Reagent MW Eq. g/mL mmol Hydroxylamine resin (1) 0.77 mmol/g 1.0 3.188 g 2.45 Fmoc-Thr(tBu)-OH 397.50 3.0 2.927 g 7.36 HATU 380.25 3.0 2.798 g 7.36 DIEA 129.25 10.0 4.3 mL 24.6 DMF 40 mL

A suspension of N-Fmoc-hydroxylamine 2-chlorotrityl resin (3.188 g, 2.45 mmol, 0.77 mmol/g, Novabiochem) in DCM (40 mL) was shaken for 2 h and drained. The resin was treated with 20% piperidine in DMF (40 mL) for 1 hour, washed with DMF (2×40 mL), treated a second time with 20% piperidine in DMF (40 mL), washed with DMF (3×40 mL) and DCM (3×40 mL) and drained completely. In a separate flask, Fmoc-Thr(tBu)-OH (2.927 g, 7.36 mmol), HATU (2.798 g, 7.36 mmol) and DIEA (4.3 mL, 24.6 mmol) were dissolved in DMF (40 mL), stirred three minutes and added to the resin. After shaking for 24 h, the mixture was drained, washed with DMF (4×40 mL) and DCM (4×40 mL) and dried in vacuo to give 3.500 g of a yellow resin.

Preparation of 4-buta-1,3-diynyl-N-(2-tert-butoxy-1-hydroxycarbamoyl-propyl)-benzamide on hydroxylainine 2-chlorotrityl resin (4)

Reagent MW Eq. g/mL mmol Fmoc-threonine/resin (2) 0.77 mmol/g 1.0 2.030 g 1.56 Butadiynyl benzoic acid (3) 170.16 2.3 0.617 g 3.63 EDCI 191.71 2.8 0.834 g 4.35 HOBt 135.13 2.8 0.588 g 4.35 DIEA 129.25 3.7 1.0 mL 5.7 DCM 15 mL DMF 4 mL

The resin 2 (2.030 g, 1.56 mmol, 0.77 mmol/g) was swelled in DCM (20 mL) for 2 h and drained. The resin was treated with 20% piperidine in DMF (20 mL) for 1 hour, washed with DMF (4×20 mL) and DCM (4×20 mL) and drained completely. In a separate flask, 4-buta-1,3-diynyl-benzoic acid 3 (0.617 g, 3.63 mmol), EDCI (0.834 g, 4.35 mmol), HOBt (0.588 g, 4.35 mmol) and DIEA (1.0 mL, 5.7 mmol) were dissolved in DCM (15 mL) and DMF (4 mL), stirred 45 min and added to the resin. After shaking for 36 h, the mixture was drained, washed with DMF (4×20 mL) and DCM (4×20 mL) and dried in vacuo to give 1.900 g of a pale brown resin.

Synthesis of Diacetylenic Threonine Hydroxamic Acids Example 22 (2S,3R)-4-[4-(3-aminomethyl-phenyl)-buta-1,3-diynyl]-N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-benzamide (3)

Reagent MW Eq. g/mL mmol Diacetylene on resin (1) 0.77 mmol/g 1.0 100 mg 0.077 3-Iodobenzylamine HCl (2) 269.51 4.0 83.0 mg 0.308 PdCl₂(PPh₃)₂ 701.89 0.2 11.0 mg 0.016 CuI 190.44 0.5 7.0 mg 0.037 Et₃N 101.19 23 250 μL 1.80 DMF 1.5 mL

Resin 1 (obtained from previous synthesis) (100 mg, 0.077 mmol) was swelled in DCM (2 mL) for 1 h and drained. A solution of 3-iodobenzylamine hydrochloride 2 (83.0 mg, 0.308 mmol) and Et₃N (250 μL, 1.80 mmol) in DMF (1.5 mL) was purged with a stream of N₂ bubbles for two minutes and added to the resin. After mixing for 5 min, PdCl₂(PPh₃)₂ (11.0 mg, 0.016 mmol) and CuI (7.0 mg, 0.037 mmol) were added and the mixture shaken for 36 h. The resin was drained, washed with DMF (4×2 mL), DCM (4×2 mL) and cleaved with 10% TFA/DCM (1.5 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (1.5 mL). The cleavage fractions were combined, treated with neat TFA (3.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-65%, 0.1% TFA, UV analysis 300 nm, 28 min) and lyophilization of the collected fractions afforded 4.3 mg (14%) of (2S,3R)-4-[4-(3-aminomethyl-phenyl)-buta-1,3-diynyl]-N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-benzamide as a white solid. LRMS (ES+) m/z 392.0 (C₂₂H₂₁N₃O₄+H requires 392.15); RP-HPLC (300 nm, 28 min run) 10.0 min.

Synthesis of Diacetylenic Benzylamine Analogues Example 23 (1S,2R)—N-2-hydroxy-1-hydroxycarbamoyl-propyl)-4-[4-(4-morpholin-4-ylmethyl-phenyl)-buta-1,3-diynyl]-benzamide (4)

Preparation of Threonine Diacetylenic Benzaldehyde on Resin (3)

Reagent MW Eq. g/mL mmol Diacetylene on resin (1) 0.77 mmol/g 1.0 1.00 g 0.770 4-Iodobenzaldehyde 232.00 4.0 715 mg 3.081 PdCl₂(PPh₃)₂ 701.89 0.07 40.0 mg 0.057 CuI 190.44 0.13 19.0 mg 0.100 Et₃N 101.19 9.3 1.00 mL 7.17 DMF 20.0 mL

Resin 1 (1.00 g, 0.77 mmol) was pre-swelled in DCM (25 mL) for 14 h and drained. A solution of 4-iodobenzaldehyde 2 (715 mg, 3.08 mmol) and Et₃N (1.00 mL, 7.17 mmol) in DMF (20 mL) was purged with N₂ for two minutes and added to the resin. After mixing for 5 min, PdCl₂(PPh₃)₂ (40.0 mg, 0.057 mmol) and CuI (19.0 mg, 0.100 mmol) were added and the reaction shaken for 48 h. The resin was drained, washed with DMF (4×20 mL), DCM (4×20 mL) and dried in vacuo to give 11.100 g of a dark yellow resin.

Preparation of (1S,2R)—N-2-hydroxy-1-hydroxycarbamoyl-propyl)-4-[4-(4-morpholin-4-ylmethyl-phenyl)-buta-1,3-diynyl]-benzamide (4)

Reagent MW Eq. mg/μl mmol Benzaldehyde on resin (3) 0.77 mmol/g 1.0 188 mg 0.141 Morpholine 87.12 6.0 75 μL 0.860 NaCNBH₃ 62.84 4.5 40 mg 0.637 Trimethyl orthoformate 106.12  6.5 100 μL 0.914 Acetic acid 60.05 12.3 100 μL 1.750 THF 3.0 mL MeOH 1.0 mL

A solution of morpholine (75 μL, 0.860 mmol) and trimethyl orthoformate (100 μL, 0.914 mmol) in THF (3.0 mL) was added to a Teflon-lined screw-capped vial containing the resin-bound diacetylenic benzaldehyde 3. The resin was agitated for 10 min, treated successively with acetic acid (100 μL, 1.75 mmol) and a solution of NaCNBH₃ (40.0 mg, 0.637 mmol) in MeOH (1.0 mL) and shaken for 44 h. The resin was filtered, washed with DMF (3×3 mL) and DCM (3×3 mL) and drained. Cleavage from the resin was achieved by treatment with 10% TFA/DCM (2.0 mL) and shaking 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (2.0 mL). The cleavage fractions were combined, treated with neat TFA (3.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude yellow residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-35%, 0.1% TFA, UV analysis 300 nm, 18 min) and lyophilization of the collected fractions afforded 19.0 mg (29%) of 472 as a fluffy yellow solid. LRMS (ES+) m/z 462.0 (C₂₆H₂₇N₃O₅+H requires 462.10); HPLC (300 nm, 18 min run) 10.3 min.

Synthesis of 4′-Benzamide Diacetylene Threonine Hydroxamic Acid Example 24 (1S,2R)—N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-4-{4-[4-(2-amino-ethylcarbamoyl)-phenyl]-buta-1,3-diynyl}-benzamide (5)

Preparation of N-(2-trityl-amino-ethyl)-4-ethynyl-benzamide (3)

Reagent MW Eq. g/mL mmol 4-Ethynylbenzoic acid (1) 146.14 1.0 0.292 g 2.00 N-Trityl ethylenediamine 302.41 1.3 0.810 g 2.67 EDCI 191.71 1.0 0.382 g 2.00 HOBt 135.13 3.0 0.270 g 2.00 DIEA 129.25 4.0 1.40 mL 8.00 DMF 10.0 mL

To a solution of 4-ethynylbenzoic acid 1 (292 mg, 2.00 mmol), EDCI (382 mg, 2.00 mmol), and HOBt (270 mg, 2.00 mmol) in DMF (10 mL) was added N-trityl ethylenediamine 2 (810 mg, 2.67 mmol) and DIEA (1.4 mL, 8.0 mmol). The reaction mixture was stirred 24 h, diluted with EtOAc (200 mL), washed with 0.5 M HCl (60 mL), saturated NaHCO₃ (2×60 mL), H₂O (4×60 mL), dried over MgSO₄ and concentrated to give 836 mg (97% yield) of N-(2-trityl-amino-ethyl)-4-ethynyl-benzamide 3 as a white solid, mp 50-51° C. R_(f)=0.40 (1:1 Hexanes/EtOAc).

Preparation of (1S,2R)—N-(2-hydroxy-1-hydroxyearbamoyl-propyl)-4-{4-[4-(2-amino-ethylcarbamoyl)-phenyl]-buta-1,3-diynyl}-benzamide (5)

Reagent MW Eq. g/mL mmol Alkyne on resin (4) 0.77 mmol/g 1.00 150 mg 0.116 4-Ethynylbenzamide (3) 430.54 3.00 151 mg 0.350 PdCl₂(PPh₃)₂ 701.89 0.25 21 mg 0.030 CuI 190.44 1.25 28 mg 0.147 Et₃N 101.19 9.50 150 μL 1.10 DMF 2.0 mL

Resin 4 (150 mg, 0.116 mmol) was swelled in DCM (2 mL) for 1 h and drained. A solution of 4-ethynylbenzamide 3 (151 mg, 0.350 mmol) and Et₃N (150 μL, 1.10 mmol) in DMF (2.0 mL) was added and the resin agitated for 5 min. A mixture of PdCl₂(PPh₃)₂ (21 mg, 0.030 mmol) and CuI (28 mg, 0.147 mmol) was added and the resin was agitated for 60 h. The resin was drained, washed with DMF (3×2 mL), DCM (3×2 mL) and cleaved with 10% TFA/DCM (1.5 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (1.0 mL). The cleavage fractions were combined, treated with neat TFA (2.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-65%, 0.1% TFA, UV analysis 300 nm, 26 min) and lyophilization of the collected fractions afforded 2.0 mg (4% yield) of (1S,2R)—N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-4-{4-[4-(2-amino-ethylcarbamoyl)-phenyl]-buta-1,3-diynyl}-benzamide. LRMS (ES+) m/z 449.1 (C₂₄H₂₄N₄O₅+H requires 449.18); RP-HPLC (300 nm, 26 min run) 17.0 min.

Synthesis of 3′-Pyridine Diacetylene Threonine Hydroxamic Acid Example 25 N-((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-4-(4-pyridin-3-yl-buta-1,3-diynyl)-benzamide (3)

Preparation of N-((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-4-(4-pyridin-3-yl-buta-1,3-diynyl)-benzamide (3)

Reagent MW Eq. g/mL mmol Alkyne on resin (1) 0.77 mmol/g 1.0 142 mg 0.109 3-Ethynylpyridine (2) 103.12 3.4 38 mg 0.368 PdCl₂(PPh₃)₂ 701.89 0.3 22 mg 0.031 CuI 190.44 1.2 25 mg 0.131 Et₃N 101.19 13 200 μL 1.40 DMF 2.0 mL

Resin 1 (142 mg, 0.109 mmol) was swelled in DCM (2 mL) for 1 h and drained. A solution of 3-ethynylpyridine 2 (38 mg, 0.368 mmol) and Et₃N (200 μL, 1.4 mmol) in DMF (2 mL) was added and the resin agitated for 5 min. A mixture of PdCl₂(PPh₃)₂ (22 mg, 0.031 mmol) and CuI (25 mg, 0.131 mmol) was added and the resin was agitated for 72 h. The resin was drained, washed with DMF (3×2 mL), DCM (3×2 mL) and cleaved with 10% TFA/DCM (1.5 mL) for 20 min. The solution was collected and the resin was rinsed with additional 10% TFA/DCM (1.0 mL). The cleavage fractions were combined, treated with neat TFA (2.0 mL), stirred for 1 h at rt and concentrated by rotary evaporation to give a crude brown residue. Purification by RP-HPLC (C₁₈ column, CH₃CN gradient 5-65%, 0.1% TFA, UV analysis 300 nm, 24 min) and lyophilization of the collected fractions afforded 4.4 mg (11% yield) of N-((2R)-hydroxy-(1S)-hydroxycarbamoyl-propyl)-4-(4-pyridin-3-yl-buta-1,3-diynyl)-benzamide. LRMS (ES+) m/z 364.0 (C₂₀H₁₇N₃O₄+H requires 364.13); RP-HPLC (300 nm, 24 min run) 11.2 min.

Example 26 Synthesis of N-(1-(N-hydroxycarbamoyl)(1S,2R)-2-hydroxy propyl){4-[4-(6-morpholin-4-yl(3-pyridyl))buta-1,3-diynyl]phenyl}carboxamide (5)

Reagent MW EQ g/ml mmol Dibromovinylbenzoic acid (1) 320 1.0 9.6 g 30.0 2-Chloro-5-ethynyl-pyridine 138 1.3 5.43 g 39.0 Pd₂dba₃ 915 0.01 274 mg  0.3 (1% cat.) TMPP 352 0.04 422 mg  1.2 (4%) TEA 101 3.0 12.5 ml 90.0 DMF 90 ml degassed with argon

Preparation of 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid methyl ester

4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid was made according to the method of Wang Shen and Sheela A. Thomas in Org. Lett. 2000, 2(18), 2857-2860.

A solution of 4-(2,2-dibromo-vinyl)-benzoic acid methyl ester (1) (9.6 g, 30.0 mmol), ethynyl-pyridine (2) (5.43 g, 39.0 mmol), Pd₂ dba₃ (274 mg, 0.3 mmol), tris(4-methoxyphenyl) phosphine (TMPP) (422 mg, 1.2 mmol) were dissolved in argon sparged (5 min.) DMF (60 ml). The reaction was sparged with argon for 1 min. TEA (12.5 ml, 90.0 mmol) was added to the stirred reaction mixture that was then heated under argon at 85° C. for 3 hours. The reaction was found complete by LCMS. The reaction was cooled to rt and diluted with EtOAc/hexane (1:1) (500 ml). The organic phase was washed with 1M NaOH (2×80 ml), water (2×80 ml), sat. brine (80 ml), dried with Na₂SO₄, filtered and concentrated under reduced pressure to give crude product. The residue was filtered through a filter plug of silica eluting with EtOAc/hexane (1:1). The fractions with product were evaporated to give 9.06 g of product in good purity (˜96% pure). The material was taken on without further purification.

Preparation of 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid (3)

A 6M aq. solution of NaOH (15 ml) was added to a stirred solution of 4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid methyl ester. (9.06 g, 30 mmol) in MeOH (350 ml) at rt. The reaction solution was heated to reflux for 3 hours. The reaction stayed a mixture and did not turn clear. HPLC and LCMS indicated that the reaction was forming side products. The reaction was cooled to rt and some MeOH (˜200 ml) was removed by evaporation under reduced pressure. Water (400 ml) was added to the mixture. Conc. HCl was added dropwise to the stirred solution until acidic by pH paper (pH2). The yellow precipitate that formed was collected by suction filtration. The solid was washed with water (3×20 ml) and hexane (2×20 ml) to give the crude product. HPLC indicated that there was approximately 40% product in the mixture. The crude reaction product was purified by flash chromatography using EtOAc (8-10%)/hexane as eluant. The pure fractions were evaporated and dried in vacuo to give 4.2 g of product 3 in 50% yield.

Preparation of [4-[4-(6-chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoyl]-HN-Thr(OtBu)-hydroxamic acid trityl resin (4)

4-[4-(6-Chloro-pyridin-3-yl)-buta-1,3-diynyl]-benzoic acid (3) was coupled to a tert-butyl protected threonine pre-loaded on hydroxylamine 2-chlorotrityl resin following the same procedure as used for Example 26. The coupling employed DIC and HOBT. [N-Fmoc-hydroxylamine 2-chlorotrityl resin was purchased from Novabiochem cat.# 01-64-0165.]

Preparation of N-(2-Hydroxy-1-hydroxycarbamoyl-propyl)-4-[4-(6-morpholin-4-yl-pyridin-3-yl)-buta-1,3-diynyl]-benzamide (5)

A solution of morpholine (300 uL) in NMP (1 ml) was added to a vial containing the 2-cloropyridine resin (4) (150 mg, 0.12 mmol). The reaction mixture was purged with argon and heated to 85-90° C. for 24 hours. The resin was drained and washed with DMF and DCM alternately several times. The product was cleaved from the resin through treatment with a TFA/water solution (80:20) (1.5 ml) for 45 min. The resin was filtered and washed with fresh TFA/water solution (80:20) (0.5 ml). The combined TFA and organic fractions were diluted with CH3CN/water (1:1) (10 ml), water (2 ml) and lyophilized. The crude product was purified by prep. HPLC. The crude product was dissolved in DMSO (1 ml), passed through a Teflon syringe filter, and the clear filtrate was injected on a preparative HPLC. The purification used a 20×50 mm Ultro 120 C18 column running a 22 ml/min 2% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness to give 2.2 mg of pure product as the TFA salt (˜32% yield).

Example 27 Synthesis of 4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-benzamide (4)

Preparation of 2-{4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-benzoylamino}-3-tert-butoxycarbonyloxy-butyric hydroxamic acid trityl resin (3)

Reagent MW EQ g/ml mmol H-Thr(Boc)-NHO- 1.0 5.8 g 4.47 Trt Resin (1) 1,3-diynyl benzoic acid (2) 261.3 1.4 1.64 g 6.25 HOBT 135.1 1.4 0.85 g 6.25 DIC 126.2 1.4 0.98 ml 6.25 DIEA 129.25 3.5 2.7 ml 15.6 DMF 50 ml

DIEA (2.7 ml, 15.6 mmol) was added to a stirred solution of 4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-benzoic acid (2) (1.64 g, 6.3 mmol), HOBT (0.85 g, 6.3 mmol), DIC (0.98 ml, 6.3 mmol) in DMF (50 ml). After 2 min., the Thr hydroxylamine resin (5.8 g, 4.5 mmol) was added in one portion. [N-Fmoc-hydroxylamine 2-chlorotrityl resin was purchased from Novabiochem cat.# 01-64-0165.] After 12 hours at rt, the reaction was found complete by LCMS. The resin was drained and washed with DMF and DCM alternately 3 times each. The product on resin 3 was used as is in subsequent reactions without further treatment.

Preparation of 4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-N-(2-hydroxy-1-hydroxy carbamoyl-propyl)-benzamide (4)

Reagent MW EQ g/ml mmol 1,3-diynyl benzoic Thr Resin (3) 1.0 120 mg 0.09 TFA/water (80:20) 1.5 ml

The product (4) (120 mg, 0.09 mmol) was cleaved from the resin through treatment with a TFA/water solution (80:20) (1.5 ml) for 45 min. The resin was filtered and washed with fresh TFA/water solution (80:20) (0.5 ml). The combined TFA and organic fractions were diluted with CH3CN/water (1:1) (10 ml), water (2 ml) and lyophilized. The crude product was purified by prep. HPLC. The crude product was dissolved in DMSO (1 ml), passed through a Teflon syringe filter, and the clear filtrate was injected on a preparative HPLC. The purification used a 20×50 mm Ultro 120 C18 column running a 22 ml/min 2% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness to give 2.2 mg of pure product as the TFA salt. The product (4) was lyophilized again from CH₃CN/water with 10 equivalents of HCl to remove most of the TFA to yield 2 mg of product as the HCl salt (˜53% yield).

Example 28 Synthesis of 4-{4-[4-(2-Dimethylamino-acetylamino)-phenyl]-buta-1,3-diynyl}-N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-benzamide (6) (Continued from compound 3 of Example 27 above)

Preparation of 2-(4-{4-[4-(2-Bromo-acetylamino)-phenyl]-buta-1,3-diynyl}-benzoylamino)-3-tert-butoxycarbonyloxy-butyric acid hydroxamate trityl resin (5)

Reagent MW EQ g/ml mmol Amino 1,3-diynyl benzoic Thr Trt Resin (3) 1.0 0.75 g 0.578 Bromo-acetyl chloride 157.4 8.0 0.728 g 4.62 Lutidine 107 10.0 1.07 ml 9.24 DMF 6 ml

A solution of bromo-acetyl chloride (0.75 g, 0.58 mmol) in DCM (2 ml) was added to a mixture of 2-{4-[4-(4-Amino-phenyl)-buta-1,3-diynyl]-benzoylamino}-3-tert-butoxycarbonyloxy-butyric acid hydroxamate Trt Resin (3) (0.75 g, 0.58 mmol), lutidine (1.1 ml, 9.2 mmol) and DCM (4 ml) at rt with shaking. After shaking for 1.5 hours, the reaction was found complete by LCMS. The resin was drained and washed with DCM (2×10 ml), DMF (3×10 ml) and DCM (3×10 ml) again. The resin was drained and dried in vacuo. The product on resin 5 was used as is in subsequent reactions without further treatment.

Preparation of 4-{4-[4-(2-Dimethylamino-acetylamino)-phenyl]-buta-1,3-diynyl}-N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-benzamide (6)

Reagent MW EQ g/ml mmol Bromo acetic Thr Trt Resin (5) 1.0 125 mg 0.093 Dimethyl amine 45.08 0.2 ml excess NMP 1.2 ml

A solution of dimethyl amine (0.2 ml) in NMP (1.2 ml) was added to bromo acetic Thr Trt Resin (5) (125 mg, 0.09 mmol) at rt with shaking. After shaking for 12 hours, the reaction was found complete by LCMS. The resin was drained and washed with DCM (2×10 ml), DMF (3×10 ml) and DCM (3×10 ml) again. The product (6) was cleaved from the resin through treatment with a TFA/water solution (80:20) (1.5 ml) for 45 min. The resin was filtered and washed with fresh TFA/water solution (80:20) (0.5 ml). The combined TFA and organic fractions were diluted with CH3CN/water (1:1) (10 ml), water (2 ml) and lyophilized. The crude product was purified by prep. HPLC. The crude product was dissolved in DMSO (1 ml), passed through a Teflon syringe filter, and the clear filtrate was injected on a preparative HPLC. The purification used a 20×50 mm Ultro 120 C18 column running a 22 ml/min 2% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness to give 2 mg of pure product as the TFA salt (˜37% yield).

Example 29 Synthesis of 4-{4-[4-(2-Amino-4-methyl-pentanoylamino)-phenyl]-buta-1,3-diynyl}-N-(2-hydroxy-1-hydroxycarbamoyl-propyl)-benzamide (7) (Continued from compound 3 of Example 27 above)

Reagent MW EQ g/ml mmol Amino 1,3-diynyl benzoic Thr Trt Resin (3) 1.0 125 mg 0.093 Fmoc-L-leucine 353.42 4.0 0.135 g 0.384 HATU 380 4.0 0.146 g 0.384 DIEA 129.25 8.0 133 ul 0.768 DMF 1.5 ml

A solution of Fmoc-L-leucine (0.135 g, 0.38 mmol), HATU (0.146 g, 0.38 mmol) in DMF (1.5 ml) was made. After 2 min. of shaking, the activated acid was added to the amino 1,3-diynyl benzoic Thr Trt Resin (3) (125 mg, 0.09 mmol) at rt with shaking. After shaking for 36 hours, the reaction was drained and washed with DCM (2×4 ml), DMF (3×4 ml) and DCM (3×4 ml) again. The resin was treated with 20% piperizine in DMF (4 ml) for 2 hours twice. The resin was drained and washed with DMF and DCM alternately several times. The product was cleaved from the resin through treatment with a TFA/water solution (80:20) (1.5 ml) for 45 min. The resin was filtered and washed with fresh TFA/water solution (80:20) (0.5 ml). The combined TFA and organic fractions were diluted with CH3CN/water (1:1) (10 ml), water (2 ml) and lyophilized. The crude product was purified by prep. HPLC. The crude product was dissolved in DMSO (1 ml), passed through a Teflon syringe filter, and the clear filtrate was injected on a preparative HPLC. The purification used a 20×50 mm Ultro 120 C18 column running a 22 ml/min 2% gradient (AcCN/water, 0.1% TFA) for 16 min. The purified fractions were lyophilized to dryness to give 1.7 mg of pure product (7) as the TFA salt (˜30% yield).

Examples 30-1307 of Table 1 were synthesized according to the synthetic schemes described above.

Biological Protocols and Data

P. aeruginosa LpxC Inhibition Assay

The assay followed the general method of Hyland et al (Journal of Bacteriology 1997 179, 2029-2037: Cloning, expression and purification of UDP-3-O-acyl-GlcNAc deacetylase from Pseudomonas aeruginosa: a metalloamidase of the lipid A biosynthesis pathway) and the radiolabeling procedure is according to Kline et al. supra. Briefly, samples were incubated with 2 nM P. aeruginosa LpxC and 150 nM [3H-Ac]-UDP-3-O—(R-3-hydroxydecanoyl)-GlcNAc in a total volume of 50 uL for 90 min at room temperature. Reactions were carried out in 96-well polypropylene plates in 50 mM sodium phosphate buffer, pH 7.5, containing 1 mg/mL BSA. Reactions were stopped by the addition of 180 uL of a 3% suspension of activated charcoal powder in 100 mM sodium acetate, pH 7.5. Supernatants were clarified by centrifugation. A portion of the clarified supernatant, containing the enzymatically released [3H]-acetate, was transferred to opaque white 96-well plates containing scintillation fluid. The radioactivity was measured in a Perkin-Elmer/Wallac Trilux Microbeta counter. Control reactions to which 5 mM EDTA had been added were included with each run to determine nonspecific tritium release.

Bacterial Screens and Cultures

Bacterial isolates were cultivated from −70° C. frozen stocks by two consecutive overnight passages at 35° C. in ambient air on 5% blood agar (Remel, Lenexa, Kans.). Clinical isolates tested were from a collection composed of isolates collected during clinical trials and recent clinical isolates obtained from various geographically diverse hospitals in the US. Quality control and primary panel strains were from the American Type Culture Collection (ATCC; Rockville, Md.), with the exception of P. aeruginosa PAO200, a strain with a deletion of the mexABoprM genes that was received from Dr. H. Schweizer. This strain does not express the principal multidrug efflux pump and is hypersusceptible to many antibacterials. Strain Z61 (ATCC 35151) is also hypersusceptible to antibacterials. It is thought that the hypersusceptibility of this strain is the result of increased permeability of its outer membrane (Angus B L et al, Antimicrobial Agents and Chemotherapy 1982 21, 299-309: Outer membrane permeability in Pseudomonas aeruginosa: Comparison of a wild-type with an antibacterial-supersusceptible mutant).

Susceptibility Testing

Minimum Inhibitory Concentrations (MICs) were determined by the broth microdilution method in accordance with the National Committee for Clinical Laboratory Standards (NCCLS) guidelines. In brief, organism suspensions were are adjusted to a 0.5 McFarland standard to yield a final inoculum between 3×10⁵ and 7×10⁵ colony-forming units (CFU)/mL. Drug dilutions and inocula were made in sterile, cation adjusted Mueller-Hinton Broth (Remel). An inoculum volume of 100 μl was added to wells containing 100 μl of broth with 2-fold serial dilutions of drug. All inoculated microdilution trays were incubated in ambient air at 35° C. for 18-24 hours. Following incubation, the lowest concentration of the drug that prevented visible growth was recorded as the MIC. Performance of the assay was monitored by the use of laboratory quality-control strains against tobramycin, that has a defined MIC spectrum, in accordance with NCCLS guidelines.

Efficacy in Mouse Model of Systemic Pseudomonas aeruginosa Infection

Female Balb/c mice were injected intraperitoneally with 0.5 ml of a bacterial suspension containing approximately 100 times the dose that would kill 50% of animals (LD₅₀) of P. aeruginosa strain PAO1 or E. coli ATCC 25922. At one and five hours post infection, the test compound was injected intravenously in doses ranging from 5 mg/kg to 100 mg/kg, five mice per group. Mice were observed for 5 days, and the dose of compound resulting in survival of 50% of mice (ED₅₀) was calculated.

Drug Combination (Synergy) Studies

I. Principle

Checkerboard experiments can be performed to assess potential interactions between primary drug of interest (#1) and other related antibacterials (#2). P. aeruginosa ATCC 27853, S. aureus ATCC 29213 and other organisms can be used as challenge strains as well as selected clinical isolates. Broth microdilution format can be used to assess the activity of drug #1 and test compound alone and in combination. Two-fold dilutions of the two compounds to be tested (each bracketing the expected MIC value) are used. The fractional inhibitory concentration (FIC) was calculated as the MIC of compound #1 in combination with a second compound, divided by the MIC of compound #1 alone. A summation FIC (ΣFIC) was computed for each drug combination as the sum of the individual FICs of compound #1 and #2. Synergy was defined as an ΣFIC ≦0.5, indifference as an ΣFIC between 0.5 and 4, and antagonism as ΣFIC >4. The lowest ΣFIC was used for the final interpretation of drug combination studies.

Interpretation of Summation (ΣFIC)

a) Synergism, x≦0.5

b) Indifference, 0.5≦x≦4

c) Antagonism, x>4

TABLE 2 Demonstration of Antibacterial activity of Select Compounds from Table 1 Enzyme inhibitory activity Compound Example # IC₅₀ (nM) 12 <100 nM 572 <100 nM 481 <100 nM 19 <100 nM 516 <100 nM 280 <100 nM 366 <100 nM 777 <100 nM 315 <100 nM 779 <100 nM 860 <100 nM 801 <100 nM 13 <100 nM

TABLE 3 Antibacterial activity vs standard panel of organisms (MIC, μg/ml). Bacterial strain: Compound P. aeruginosa E. coli S. aureus hyper-permeable P. aeruginosa Example # 27853 25922 29213 P. aerug. 35151 PAO200 mexAB 12 A A C A A 572 A A C A A 481 A A C A A 19 A A B A A 516 A A C A A 280 A A C A A 366 A A C A A 777 A A C A A 315 A A C A A 779 A A C A A 860 A A C A A 801 A A C A A 13 A A C AA A MIC Key MIC's of 6.25 ug/ml or less = A MIC's of greater than 6.25 ug/ml to 50 ug/ml = B MIC's of greater than 50 ug/ml = C

TABLE 4 Antibacterial activity vs cystic fibrosis isolates of Pseudomonas aeruginosa (MIC, μg/ml). Strains have the following phenotypes: 3198 and 3236, sensitive to most antibacterials; 2196, resistant to ciprofloxacin; 3224, resistant to ceftazidime; 3317, resistant to aztreonam; 1145 and 3206, multi-drug resistant. Strain number: 3198 3236 2196 3224 3232 3317 1145 3206 Phenotype: LpxC inhibitors Sensitive Sensitive Cipro R Tobra R Ceftaz. R Aztr. R MDR MDR 12 A A B A A A A A 481 A A A A A A A A 19 A A A A A A A A 516 A A A A A A A A 280 A A B A A A A A 366 A A A A A A A A 777 A A A A A A A A 315 A A A A A A A A 779 A A A A A A A A 801 A A A A A A A A 13 A A A A A A A A Comparator antibacterials Tobramycin 2 0.5 2 64 1 2 8-32 64 Aztreonam 1 0.5 1 1 1 64 >128 >128 Ceftazidime 2 0.25 2 2 64 4 >128 >128 Cefepime 4 2 2 8 2 8 >128 32 Ciprofloxacin 1 0.06 >8 2 2 0.5 4 >8 MIC Key MIC's of 6.25 ug/ml or less = A MIC's of greater than 6.25 ug/ml to 50 ug/ml = B MIC's of greater than 50 ug/ml = C

TABLE 5 Antibacterial activity vs non-CF clinical isolates of P. aeruginosa and vs other gram-negative pathogens. Set 1: non-fermenting organisms. P. aer., P. aeruginosa; Acinet. calc., Acinetobacter calcoaceticus; Alcal. xyl., Alcaligenes xylosoxidans; B. cep., Burkholderia cepacia; S. malt., Stenotrophomonas maltophilia Species: LpxC inhibitors P. aer 27853 P. aer. PAO1 P. aer 12307 P. aer psa-6b Acinet. calc. Alcal. xyl B. cepacia S. malt. 12 A A A A A A B A 481 A A A A C C B C 19 A A A A A B B B 516 A A A C C C C 280 A A A A C B B B 366 A A A B C A B B 777 A A B A B A C 315 A A A A C B A A 779 A A A C A A B 801 A A A B C B C 13 A A A C A A B Comparator antibacterials Tobramycin 8 2 2 64  64/>128 0.5 Aztreonam 16 32 32 32 64 >128/16 Ceftazidime 4 64 16 1 8/4 1 Cefepime 2 8 8 8 32/16  8/1 Meropenem 0.5 0.25 4 0.5 4 64 Pip/Tazo 4 >128 8 1 64 16 Ciprofloxacin 0.5 2 0.5 0.5 MIC Key MIC's of 6.25 ug/ml or less = A MIC's of greater than 6.25 ug/ml to 50 ug/ml = B MIC's of greater than 50 ug/ml = C

TABLE 6 Antibacterial activity vs non-CF clinical isolates of P. aeruginosa and vs other gram- negative pathogens, continued. Set 2: enteric organisms. E. aer., Enterobacter aerogenesP; E. clo., Enterobacter cloacae; E. coli, Escherichia coli; K. pneu., Klebsiella pneumoniae; K. oxy., Klebsiella oxytoca; P. mir., Proteus mirabilis; S. marc., Serratia marcescens. Species: LpxC inhibitors E. aer. E. clo. E. coli 1619 E. coli 2788 K. pneu. K. oxy. P. mir. S. marc. 12 C A A A A A A A 481 C A A A A A A A 19 A A A A A A A A 516 C B A B C C C A 280 C A A A B C B B 366 C A A A B B A A 777 B A A A A A A A 315 C A A A C C C B 779 C A A A B B B A 801 B A A A A A A A 13 C A A A A A A A Comparator antibacterials Tobramycin 64 0.06 16/64 0.06/2  64 1 2 2 Aztreonam <=0.13 128/64  <=0.13/0.25 2 0.5 <=0.13 <=0.13 Ceftazidime 32 0.25 >128   0.25/<=0.13 8 0.25 <=0.13 0.25 Cefepime <=0.13    4/<=0.13 <=0.13 8 <=0.13 <=0.13 <=0.13 Meropenem 2 <=0.06 0.25/0.13 <=0.06 0.13 <=0.06 0.5 0.13 Pip/Tazo 2 >128 1 >128 2 0.25 1 Ciprofloxacin >8 0.015 2 0.03 0.06 0.03 0.03 0.25 MIC Key MIC's of 6.25 ug/ml or less = A MIC's of greater than 6.25 ug/ml to 50 ug/ml = B MIC's of greater than 50 ug/ml = C

TABLE 7 Drug Combination (Synergy) Studies Result Minimum Concentration (mg/ml) required to inhibit grouth of E. coli 25922 Erythromycin LpxC inhibitor 925 LpxC inhibitor 925 only — 6.25 Erythromycin only 128 — LpxC inhibitor 925 + erythromycin 2 0.78

Each of the Example compounds of Table 1 was synthesized and assayed as described above. Many of the Example compounds 1-1307 displayed an IC₅₀ value of less than 10 μM with respect to LpxC. Many of these compounds displayed an IC₅₀ value of less than or equal to 1 μM or less than or equal to 0.1 μM. Many of these compounds exhibited IC₅₀ values of less than or equal to 0.050 μM, less than or equal to 0.030 μM, less than or equal to 0.025 μM, or less than or equal to 0.010 μM.

It should be understood that the organic compounds according to the invention may exhibit the phenomenon of tautomerism. As the chemical structures within this specification can only represent one of the possible tautomeric forms, it should be understood that the invention encompasses any tautomeric form of the drawn structure.

TABLE 1 Example Structure Name MH+ 30

3,4-difluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-benzamide 275.2 31

(2S,3R)-N,3-dihydroxy-2-[(4- phenylbutanoyl)amino]butanamide 281.3 32

(2S,3R)-N,3-dihydroxy-2-({4-[4- (methyloxy)phenyl]butanoyl}amino)-butanamide 311.3 33

N-{(1S,2R)-2-hydroxy-2- [(hydroxyamino)carbonyl]propyl}-5-phenylpentanamide 295.3 34

(2E,4E)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5- phenylpenta-2,4-dienamide 291.3 35

(2E)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3- phenylprop-2-enamide 265.3 36

(2S,3R)-3-hydroxy-2-({(2E)-3-[4- (methyloxy)phenyl]prop-2-enoyl}amino)butanoic acid 280.3 37

(3R)-3-amino-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]propyl}- 5-phenylpentanamide 310.4 38

(2E)-3-(4-fluorophenyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}prop-2-enamide 283.3 39

(2E)-3-(3-bromophenyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]-propyl}prop-2-enamide 344.2 40

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[(2phenylethyl)amino]- methyl}benzamide 372.4 41

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-{[(4-phenylbutyl)amino]- methyl}benzamide 400.5 42

4-[(cyclopropylamino)methyl]-N- {(1S,2R)-2-hydroxy-1-[(hydroxy- amino)-carbonyl]propyl}benzamide 308.3 43

4-[(hexylamino)methyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)-carbonyl]- propyl}benzamide 352.4 44

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[(2-pyridin-2- ylethyl)amino]methyl}benzamide 373.4 45

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(4-methylpiperazin-1-yl)- benzamide 337.4 46

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(piperidin-1-ylmethyl)benzamide 336.4 47

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (morpholin-4-ylmethyl)benzamide 338.4 48

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- ({[3-(2-oxopyrrolidin-1- yl)propyl]amino}methyl)benzamide 393.5 49

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- {[(3-phenylpropyl)amino]methyl}- benzamide 386.5 50

(2S,5R)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5- phenylpyrrolidine-2-carboxamide 308.3 51

(2R,5S)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5- phenylpyrrolidine-2-carboxamide 308.3 52

(2S,3R)-2-{[(3S)-3-amino-4- phenylbutanoyl]amino}-N,3- dihydroxybutanamide 296.3 53

(2S,3R)-2-{[(2S)-2-amino-4- phenylbutanoyl]amino}-N,3- dihydroxybutanamide 296.3 54

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 6-(2-pyrrolidin-1-ylethyl)pyridine- 3-carboxamide 337.4 55

2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-3-hydroxy-3- methylbutanoic acid 342.4 56

2-{[4-(4-ethylphenyl)phenyl]car- bonylamino}-3-hydroxy-4- methylpentanoic acid 356.4 57

{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}(thien-2-yl)acetic acid 366.5 58

N-(2-{[(1,1-dimethylethyl)oxy]- amino}-2-oxo-1-thien-2-ylethyl)- 4′-ethyl-1,1′-biphenyl-4- carboxamide 437.6 59

3-(dimethylamino)-2-{[(4′-ethyl- 1,1′-biphenyl-4-yl)carbonyl]- amino}-propanoic acid 341.4 60

4′-ethyl-N-{(1S)-1-[({(1S,2R)-2- hydroxy-1[(hydroxyamino)car- bonyl]propyl}amino)carbon- yl]-3-methyl-butyl}-1,1′-bi- phenyl-4-carboxamide 456.6 61

4′-ethyl-N-[(1S)-2-({(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]-propyl}amino)-2-oxo- 1-(phenyl-methyl)ethyl]-1,1′- biphenyl-4-carboxamide 490.6 62

(2S)-1-[(4′-ethyl-1,1′-biphenyl-4-yl)- carbonyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- pyrrolidin-2-carboxamide 440.5 63

4′-ethyl-N-[(1S)-2-({(1S,2R)-2-hy- droxy-1[(hydroxyamino)carbonyl]- propyl}amino)-1-(1H-imidazol-4- ylmethyl)-2-oxoethyl]-1,1′- biphenyl-4-carboxamide 480.5 64

(3S)-2-[(4′-ethyl-1,1′-biphenyl-4-yl)- car-bonyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,2,3,4-tetrahydroisoquinoline-3- carboxamide 502.6 65

(2S)-2-[(1,1′-biphenyl-4-ylacetyl)- amino]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-methylpentanamide 442.5 66

(2S,3R)-2-({(2S)-2-[(1,1′-biphenyl- 4-ylacetyl)amino]-3-phenylpropanoyl}amino)- N,3-dihydroxybutanamide 476.5 67

(2S,3R)-2-{[(2S)-2-[(1,1′-biphenyl- 4-ylacetyl)amino]-3-(4-hydroxy- phenyl)-propanoyl]amino}-N,3- dihydroxybutanamide 492.5 68

(2S)-1-(1,1′-biphenyl-4-ylacetyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}pyrrolidin-2-carboxamide 426.5 69

(2S,3R)-2-{[(2S)-2-[(1,1′-biphenyl- 4-ylacetyl)amino]-3-(1H-imidazol- 4-yl)propanoyl]amino}-N,3- dihydroxybutanamide 466.5 70

(2S)-2-[(1,1′-biphenyl-4-ylacetyl)- amino]-N~1~-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)car- bonyl]propyl}pentanamide 457.5 71

(3S)-3-[(1,1′-biphenyl-4-ylacetyl)- amino]-4-({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}amino)-4-oxobutanoic acid 444.5 72

(2S,4R)-1-[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]-4-hydroxy-N- {(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}- pyrrolidine-2-carboxamide 456.5 73

N-[(1S)-1-(aminomethyl)-2- ({(1S,2R)-2-hydroxy-1- [(hydroxyamino)car- bonyl]propyl}amino)-2- oxoethyl]-4′-ethyl-1,1′-biphenyl- 4-carboxamide 429.5 74

4′-ethyl-N-{(1S)-1-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)car- bonyl]propyl}amino)carbon- yl]but-3-ynyl}-1,1′-biphenyl-4- carboxamide 438.5 75

(2S,3R)-2-({(2S)-2-[(1,1′-biphenyl- 4-ylacetyl)amino]propanoyl}- amino)-N,3-dihydroxybutanamide 400.4 76

(2S,4R)-1-(1,1′-biphenyl-4-yl- acetyl)-4-hydroxy-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}pyrrolidine- 2-carboxamide 442.5 77

4′-ethyl-N-{(1R,2R)-2-hydroxy- 1-[(hydroxy{[(2-hydroxyethyl)- amino]-carbonyl}amino)methyl]- propyl}-1,1′-biphenyl-4- carboxamide 416.5 78

N-((2R,3R)-2-{[(4′-ethyl-1,1′-bi- phenyl-4-yl)carbonyl]amino}-3- hydroxybutyl)-N-hydroxymor- pholine-4-carboxamide 442.5 79

N-((2R,3R)-2-{[(4′-ethyl-1,1′-bi- phenyl-4-yl)carbonyl]amino}-3- hydroxybutyl)-N-hydroxy-4- methylpiperazine-1-carboxamide 455.6 80

N-((1R,2R)-1- {[[(cyclopropyl- amino)carbonyl](hydroxy)- amino]-methyl}-2-hydroxy- propyl)-4′-ethyl-1,1′- biphenyl-4-carboxamide 412.5 81

4′-ethyl-N-{(1R,2R)-2-hydroxy-1- [(hydroxy{[(pyridin-3- ylmethyl)amino]carbonyl}- amino)methyl]propyl}- 1,1′-biphenyl-4-carboxamide 463.5 82

4′-ethyl-N-{(1R,2R)-2-hydroxy-1- [(hydroxy{[(2-pyridin-2- ylethyl)amino]carbonyl}amino)- methyl]propyl}- 1,1′-biphenyl-4-carboxamide 477.6 83

4′-ethyl-N-{(1R,2R)-2-hydroxy-1- [(hydroxy{[(4-morpholin-4- ylphenyl)amino]carbonyl}amino)- methyl]propyl}- 1,1′-biphenyl-4-carboxamide 533.6 84

N~1~-((2R,3R)-2-{[(4′-ethyl-1,1′- biphenyl-4-yl)carbonyl]amino}- 3-hydroxybutyl)-N~1~- hydroxypiperidine-1,4-dicarboxamide 483.6 85

4′-ethyl-N-[2-(hydroxyamino)- ethyl]-1,1′-biphenyl-4- carboxamide 285.4 86

N-{2-[(aminocarbonyl)(hydroxy)- amino]ethyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 328.4 87

N-{2-[(aminocarbonothioyl)- (hydroxy)-amino]ethyl}-4′- ethyl-1,1′-biphenyl-4-car- boxamide 344.4 88

N-{2-[({[2- (dimethylamino)ethyl]- amino}carbonyl)(hydroxy)- amino]ethyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 399.5 89

N-{2-[{[(2- cyanoethyl)amino]carbonyl}- (hydroxy)amino]-ethyl}-4′- ethyl-1,1′-biphenyl-4- carboxamide 381.4 90

4′-ethyl-N-[2-(hydroxy{[(2- hydroxyethyl)amino]car- bonyl}amino)ethyl]- 1,1′-biphenyl-4-carboxamide 372.4 91

N-(2-{[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]amino}ethyl)-N- hydroxymorpholine-4-carboxamide 398.5 92

N-(2-{[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]amino}ethyl)- N-hydroxy-4-methylpiperazine- 1-carboxamide 411.5 93

N~1~-(2-{[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]amino}ethyl)- N~1~-hydroxypiperidine-1,4- dicarboxamide 439.5 94

N-(2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}ethyl)-N- hydroxypyrrolidine-1-carboxamide 382.5 95

N-{2-[[(cyclopropylamino)- carbonyl](hydroxy)amino]- ethyl}-4′-ethyl-1,1′-biphenyl-4-carboxamide 368.4 96

4′-ethyl-N-{2-[hydroxy({[2- (methyloxy)ethyl]amino}- carbonyl)amino]ethyl}- 1,1′-biphenyl-4-carboxamide 386.5 97

N-{2-[({[2-(acetylamino)ethyl]- amino}carbonyl)(hydroxy)- amino]ethyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 413.5 98

4′-ethyl-N-{2-[hydroxy({[3- (2-oxopyrrolidin-1- yl)propyl]amino}carbonyl)- amino]ethyl}-1,1′- biphenyl-4-carboxamide 453.6 99

4′-ethyl-N-[2-(hydroxy{[(3- hydroxypropyl)amino]carbonyl}- amino)ethyl]-1,1′-biphenyl-4- carboxamide 386.5 100

4′-ethyl-N-{2-[hydroxy({[3- (methyloxy)propyl]amino}- carbonyl)amino]ethyl}- 1,1′-biphenyl-4-carboxamide 400.5 101

N-(2-{[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]amino}ethyl)- N-hydroxy-1,4′- bipiperidine-1′-carboxamide 479.6 102

4′-ethyl-N-[2-(hydroxy{[(2- pyridin-2-ylethyl)amino]- carbonyl}amino)ethyl]-1,1′- biphenyl-4-carboxamide 433.5 103

4′-ethyl-N-[2-(hydroxy{[(pyridin- 3-ylmethyl)amino]carbonyl}- amino)ethyl]-1,1′- biphenyl-4-carboxamide 419.5 104

4′-ethyl-N-[2-(hydroxy{[(4- morpholin-4-ylphenyl)amino]- carbonyl}amino)ethyl]-1,1′- biphenyl-4-carboxamide 489.6 105

N-(2-{[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]amino}ethyl)- N,3-dihydroxypiperidine-1- carboxamide 412.5 106

N-{2-[{[(3-aminocyclohexyl)- amino]carbonyl}(hydroxy)- amino]ethyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 425.5 107

N-{2-[{[(2-aminoethyl)amino]- carbonyl}(hydroxy)amino]- ethyl}-4′-ethyl-1,1′-biphenyl-4- carboxamide 371.4 108

N-{2-[{[(3- aminopropyl)- amino]carbonyl}(hydroxy)- amino]-ethyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 385.5 109

1,1-dimethylethyl 3-({[(2-{[(4′- ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}ethyl)- (hydroxy)amino]- carbonyl}amino)propylcarbamate 485.6 110

4′-ethyl-N-{2-[({[(4-fluoro- phenyl)methyl]amino}carbonyl)- (hydroxy)-amino]ethyl}-1,1′- biphenyl-4-carboxamide 436.5 111

N-(2-{[(4′-ethyl-1,1′-biphenyl- 4-yl)-carbonyl]amino}ethyl)- N-hydroxy-3-[(trifluoroacetyl)- amino]pyrrolidine-1- carboxamide 493.5 112

N-{2-[{[(4-aminothien-3- yl)amino]carbonyl}(hydroxy)- amino]-ethyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 425.5 113

4′-ethyl-N-(2-{hydroxy[(piper- idin-3-ylamino)carbonyl]- amino}ethyl)-1,1′-biphenyl- 4-carboxamide 411.5 114

4′-ethyl-N-(2-{hydroxy[(piperidin- 4-ylamino)carbonyl]amino}ethyl)- 1,1′-biphenyl-4-carboxamide 411.5 115

4′-ethyl-N-[2-(hydroxy{[(piperidin- 2-ylmethyl)amino]carbonyl}- amino)ethyl]-1,1′- biphenyl-4-carboxamide 425.5 116

4′-ethyl-N-[2-(hydroxy{[(piper- idin-3-ylmethyl)amino]carbonyl}- amino)ethyl]-1,1′-biphenyl-4- carboxamide 425.5 117

3-amino-N-(2-{[(4′-ethyl-1,1′- biphenyl-4-yl)carbonyl]amino}- ethyl)-N-hydroxypyrrolidine-1- carboxamide 397.5 118

1,1-dimethylethyl 3-[({[(2- {[(4′-ethyl- 1,1′-biphenyl-4-yl)carbonyl]- amino}-ethyl)(hydroxy)amino]- carbonyl}amino)methyl]- piperidine-1-carboxylate 525.7 119

1,1-dimethylethyl 1-{[(2-{[(4′- ethyl-1,1′-biphenyl-4-yl)car- bonyl]amino}-ethyl)(hy- droxy)amino]carbonyl}- pyrrolidin-3-ylcarbamate 497.6 120

4′-ethyl-N-[(1S,2R)-2-hy- droxy-1-({[2-(hydroxy- amino)ethyl]amino}car- bonyl)-propyl]-1,1′-biphenyl- 4-carboxamide 386.5 121

N-{(1S,2R)-1-[({2- [(aminocarbonyl)(hydroxy)- amino]ethyl}-amino)- carbonyl]-2-hydroxypropyl}- 4′-ethyl-1,1′-biphenyl-4- carboxamide 429.5 122

N-{(1S,2R)-1-[({2-[(amino- carbonothioyl)(hydroxy)amino]ethyl}- amino)carbonyl]-2-hydroxypropyl}-4′- ethyl-1,1′-biphenyl-4-carboxamide 445.6 123

4′-ethyl-N-[(1S,2R)-2-hydroxy-1-({[2- (hydroxy{[(2-hydroxy- ethyl)amino]carbonyl}amino)ethyl]- amino}carbonyl)propyl]-1,1′-biphenyl- 4-carboxamide 473.5 124

4′-ethyl-N-{(1S)-6-hydroxy-1-[(1R)-1- hydroxyethyl]-2,7-dioxo-11-oxa-3,6,8- triazadodec-1-yl}-1,1′-biphenyl-4- carboxamide 487.6 125

4′-ethyl-N-{(1S)-6-hydroxy-1-[(1R)-1- hydroxyethyl]-11-methyl-2,7-dioxo- 3,6,8,11-tetraazadodec-1-yl}-1,1′- biphenyl-4-carboxamide 500.6 126

4′-ethyl-N-{(1S)-6-hydroxy-1-[(1R)-1- hydroxyethyl]-2,7,12-trioxo-3,6,8,11- tetraazatridec-1-yl}-1,1′-biphenyl-4- carboxamide 514.6 127

4′-ethyl-N-{(1S,2R)-2-hydroxy-1-[({2- [hydroxy({[3-(2-oxopyrrolidin-1- yl)propyl]amino}carbonyl)amino]ethyl}amino)- carbonyl]propyl}-1,1′-biphenyl-4- carboxamide 554.7 128

N-{(1S,2R)-1-[({2-[{[(2- cyanoethyl)amino]carbonyl}(hydroxy)amino]- ethyl}amino)carbonyl]-2-hydroxypropyl}-4′- ethyl-1,1′-biphenyl-4-carboxamide 482.6 129

N-{(1S,2R)-1-[({2-[[(cyclo- propylamino)carbonyl](hydroxy)amino]- ethyl}amino)carbonyl]-2-hydroxypropyl}-4′- ethyl-1,1′-biphenyl-4-carboxamide 469.6 130

N-{2-[((2S,3R)-2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-3- hydroxybutanoyl)amino]ethyl}-N- hydroxypyrrolidine-1-carboxamide 483.6 131

N-{2-[((2S,3R)-2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-3- hydroxybutanoyl)amino]ethyl}-N- hydroxymorpholine-4-carboxamide 499.6 132

N-{2-[((2S,3R)-2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-3- hydroxybutanoyl)amino]ethyl}-N-hydroxy-4- methylpiperazine-1-carboxamide 512.6 133

4′-ethyl-N-[(1S,2R)-2-hydroxy-1-({[2- (hydroxy{[(pyridin-3- ylmethyl)amino]carbonyl}amino)ethyl]amino}- carbonyl)propyl]-1,1′-biphenyl-4-carboxamide 520.6 134

4′-ethyl-N-[(1S,2R)-2-hydroxy-1-({[2- (hydroxy{[(2-pyridin-2- ylethyl)amino]carbonyl}amino)ethyl]amino}- carbonyl)propyl]-1,1′-biphenyl-4-carboxamide 534.6 135

3-chloro-N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [(trifluoromethyl)oxy]benzamide 357.7 136

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[(3- nitrophenyl)methyl]oxy}benzamide 390.4 137

(4R)-2-(4-fluoro-3-prop-2-enylphenyl)-N- hydroxy-4,5-dihydro-1,3-oxazole-4- carboxamide 265.3 138

3-fluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (methyloxy)benzamide 287.3 139

4-(but-3-enyloxy)-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}benzamide 309.3 140

3-bromo-5-fluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(prop- 2-enyloxy)benzamide 392.2 141

4-fluoro-N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3- prop-2-enylbenzamide 297.3 142

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (prop-2-enyloxy)-3-(trifluoromethyl)- benzamide 363.3 143

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (methyloxy)benzamide 269.3 144

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3- (phenyloxy)benzamide 331.3 145

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (methyloxy)-3- [(trifluoromethyl)oxy]benzamide 353.3 146

N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [(trifluoromethyl)oxy]benzamide 323.2 147

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [(trifluoromethyl)oxy]benzamide 323.2 148

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (trifluoromethyl)benzamide 307.2 149

3,4-difluoro-N-{(2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 275.2 150

N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (methyloxy)benzamide 269.3 151

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′-propyl- 1,1′-biphenyl-4-carboxamide 357.4 152

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′-propyl- 1,1′-biphenyl-4-carboxamide 357.4 153

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [trifluoro(methylidene)-lambda~6~- sulfanyl]benzamide 341.3 154

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 239.2 155

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-1,1′- biphenyl-4-carboxamide 315.3 156

3-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (methyloxy)benzamide 348.2 157

4-fluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3-(prop-2- enyloxy)benzamide 313.3 158

2,3,5,6-tetrafluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-prop-2- enylbenzamide 351.3 159

3-fluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5- (trifluoromethyl)benzamide 325.2 160

4-bromo-2-fluoro-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]propyl}- benzamide 336.1 161

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (phenyloxy)benzamide 331.3 162

4-(dimethylamino)-N-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)carbonyl]- propyl}benzamide 282.3 163

2-[3-fluoro-4-(methyloxy)-5-prop-2- enylphenyl]-N-hydroxy-4,5-dihydro-1,3- oxazole-4-carboxamide 295.3 164

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5-[3- (trifluoromethyl)phenyl]furan-2-car- boxamide 373.3 165

4-{[(1E)-1,2-difluorobuta-1,3-dienyl]- oxy}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 343.3 166

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- quinoline-2-carboxamide 290.3 167

N-[2-(hydroxyamino)-1-(hydroxy- methyl)-2-oxoethyl]-1,1′-biphenyl- 4-carboxamide 301.3 168

N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 315.3 169

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-2′- methyl-1,1′-biphenyl-4-carboxamide 329.4 170

N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (trifluoromethyl)benzamide 307.2 171

4-fluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3- (trifluoromethyl)benzamide 325.2 172

N-{(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}-4-{[(3- nitrophenyl)oxy]methyl}benzamide 390.4 173

N-[(1R)-2-(hydroxyamino)-1- (mercaptomethyl)-2-oxoethyl]-4- [(trifluoromethyl)oxy]benzamide 325.3 174

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,3-benzodioxole-5-carboxamide 283.3 175

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-6- (trifluoromethyl)pyridine-3-carbox- amide 308.2 176

N-{3-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [(trifluoromethyl)oxy]benzamide 323.2 177

N-{3-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 315.3 178

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [(hydroxy(phenyl)methyl]benzamide 345.4 179

N-{(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}-4-[({4- [(trifluoromethyl)oxy]phenyl}oxy)- methyl]benzamide 429.4 180

4-[({4-bromo-2-[(tri- fluoromethyl)oxy]phenyl}oxy)- methyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 508.3 181

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-3′-nitro-1,1′- biphenyl-4-carboxamide 360.3 182

4-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 318.1 183

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4′-(methyloxy)-1,1′-biphenyl-4- carboxamide 345.4 184

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′- [(trifluoromethyl)oxy]-1,1′-biphenyl-4- carboxamide 399.3 185

4′-(ethyloxy)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-1,1′- biphenyl-4-carboxamide 359.4 186

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{5-[(Z)- (hydroxyimino)methyl]thien-2-yl}benzamide 364.4 187

3′-(ethyloxy)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-1,1′- biphenyl-4-carboxamide 359.4 188

(2R,3R)-N,3-dihydroxy-1-({4- [(trifluoromethyl)oxy]phenyl}carbonyl)pyrroli- dine-2-carboxamide 335.2 189

N-[2-(hydroxyamino)-1-(hydroxymethyl)-2- oxoethyl]-3-(1-methylethyl)-4- (methyloxy)benzamide 297.3 190

N-[2-(hydroxyamino)-1-(hydroxymethyl)-2- oxoethyl]-3-(1-methylethyl)-4-(prop-2- enyloxy)benzamide 323.4 191

N-[2-(hydroxyamino)-1-(hydroxymethyl)-2- oxoethyl]-4-(methyloxy)-3-propylbenzamide 297.3 192

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′- (methylthio)-1,1′-biphenyl-4-carboxamide 361.4 193

5-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}thio- phene-2-carboxamide 324.2 194

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-5-{4-[(trifluoro- methyl)oxy]phenyl}thiophene- 2-carboxamide 405.4 195

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-1-benzofuran-2- carboxamide 279.3 196

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-5-phenylthiophene- 2-carboxamide 321.4 197

4′-(dimethylamino)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-1,1′-biphenyl-4- carboxamide 358.4 198

(2S,3R)-N,3-dihydroxy-2-[({2- [(trifluoromethyl)oxy]phenyl}- acetyl)amino]-butanamide 337.3 199

5-[4-(ethyloxy)phenyl]-N- {(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]- propyl}thiophene-2- carboxamide 365.4 200

5-[3-(ethyloxy)phenyl]-N- {(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]- propyl}thiophene-2- carboxamide 365.4 201

(4R)-N-hydroxy-2-{2′-[(tri- fluoromethyl)-oxy]-1,1′- biphenyl-4-yl}-4,5-dihydro- 1,3-oxazole-4-carboxamide 367.3 202

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4′-(hydroxymethyl)- 1,1′-biphenyl-4- carboxamide 345.4 203

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{5-[(4-methyl- piperazin-1-yl)methyl]- thien-2-yl}benzamide 433.5 204

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-(methyloxy)- phenyl]carbonyl}- benzamide 373.4 205

N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}-4-[(E)-phenyldia- zenyl]benzamide 343.4 206

(4R)-N-hydroxy-2-{4- (methyloxy)-3-[(trifluoro- methyl)oxy]phenyl}-4,5- dihydro-1,3-oxazole-4- carboxamide 321.2 207

4′-ethyl-N-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)- carbonyl]propyl}-1,1′-bi- phenyl-4-carboxamide 343.4 208

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4′-(trifluoromethyl)- 1,1′-biphenyl-4-carboxamide 383.3 209

5-(4-ethylphenyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]-propyl}thiophene-2- carboxamide 349.4 210

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 5-[4-(methyloxy)phenyl]thiophene- 2-carboxamide 351.4 211

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-5-[4-(methylthio)- phenyl]thiophene-2- carboxamide 367.5 212

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5-(3- nitrophenyl)thiophene-2-carboxamide 366.4 213

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-oxo-4H-chromene-2-carboxamide 307.3 214

N-[1-[(hydroxyamino)carbonyl]-1- (hydroxymethyl)-2-methylpropyl]-4- [(trifluoromethyl)oxy]benzamide 351.3 215

N-[2-hydroxy-3-(hydroxyamino)-3- oxopropyl]-1,1′-biphenyl-4-car- boxamide 301.3 216

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-[(E)-2-phenylethenyl]benzamide 341.4 217

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-9H- fluorene-2-carboxamide 327.4 218

4′-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- amino)carbon-yl]-1,1′-biphenyl-4- carboxylic acid 359.3 219

N-[2-(hydroxyamino)-1-(hydroxy- methyl)-2-oxoethyl]-4-(prop-2- enyloxy)-3-propylbenzamide 323.4 220

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-iodobenzamide 365.1 221

4′-hydroxy-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-1,1′- biphenyl-4-carboxamide 331.3 222

6-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- pyridine-2-carboxamide 319.1 223

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-6- phenylpyridine-2-carboxamide 316.3 224

4′-butyl-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 371.4 225

4′-(1,1-dimethylethyl)-N-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)carbonyl]- propyl}-1,1′-biphenyl-4-carboxamide 371.4 226

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-5- [3-(methyloxy)phenyl]thiophene-2- carboxamide 351.4 227

4′-[({(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}amino)carbon- yl]-1,1′-biphenyl-4- yl dihydrogen phosphate 411.3 228

N-ethyl-N′-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-1,1′- biphenyl-4,4′-dicarboxamide 386.4 229

N-[(1S,2R)-1-(hydrazinocarbonyl)-2- hydroxypropyl]-4′-propyl-1,1′-bi- phenyl-4-carboxamide 356.4 230

N-{(1S,2R)-2-hydroxy-1- [(methylamino)carbonyl]propyl}- 4′-propyl-1,1′-biphenyl-4-carboxamide 355.4 231

N-[(1S,2R)-1-(hydrazinocarbonyl)-2- hydroxypropyl]-4-(methyloxy)- benzamide 268.3 232

(2S,3R)-2-[(1,1′-biphenyl-4-ylsulfonyl)- amino]-N,3-dihydroxybutanamide 351.4 233

4-hydroxy-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 255.2 234

3′-cyano-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 340.3 235

1,1-dimethylethyl ({4-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}amino)carbon-yl]phenyl}- oxy)acetate 369.4 236

(2S,3R)-2-[(1,1′-biphenyl-4- ylsulfonyl)(methyl)amino]-N,3- dihydroxybutanamide 365.4 237

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3′-[(Z)- (hydroxyimino)methyl]-4′-(methyloxy)-1,1′- biphenyl-4-carboxamide 388.4 238

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- [(phenylcarbonyl)amino]benzamide 358.4 239

N-hydroxy-2-[3-(1-methylethyl)-4- (prop-2-enyloxy)phenyl]-4,5-dihydro- 1,3-oxazole-4-carboxamide 305.3 240

4′-butyl-N-{(1S,2R)-2-hydroxy-1- [(methylamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 369.5 241

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(5-methylpyridine-2-yl)- benzamide 330.4 242

5-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- pyridine-3-carboxamide 319.1 243

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-pyridin-3-ylbenzamide 316.3 244

N-{(1R,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-N′- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4,4′-dicarboxamide 475.5 245

(2S,3R)-N,3-dihydroxy-2-[({4-[(E)-2- phenylethenyl]phenyl}methyl)amino]- butanamide 327.4 246

4-{[(4-bromophenyl)sulfonyl]amino}- N-{(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}benzamide 473.3 247

1,1-dimethylethyl 4-({4-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}amino)carbon-yl]phenyl}amino)- 4-oxobutylcarbamate 439.5 248

4-[(4-aminobutanoyl)amino]-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)carbonyl]- propyl}benzamide 339.4 249

1,1-dimethylethyl {4′-[({(1S,2R)-2- hydroxy[(hydroxyamino)carbonyl]- propyl}amino)meth-yl]-1,1′-bi- phenyl-4-yl}methylcarbamate 430.5 250

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- pyrimidin-5-ylbenzamide 317.3 251

1,1-dimethylethyl 5-{4-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}amino)carbon- yl]phenyl}pyridine-3-carboxylate 416.4 252

5-{4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- amino)carbonyl]phenyl}pyridine- 3-carboxylic acid 360.3 253

(4S)-N-hydroxy-2-{4-(methyloxy)-3- [(trifluoromethyl)oxy]phenyl}-4,5- dihydro-1,3-oxazole-4-carboxamide 321.2 254

(2S,3R)-2-({[4′-(aminomethyl)-1,1′-bi- phenyl-4-yl]methyl}amino)-N,3- dihydroxybutanamide 330.4 255

(3S)-1-hydroxy-3-[(1R)-1-hydroxy- ethyl]-4-({4-[(E)-2-phenylethenyl]- phenyl}methyl)piperazine-2,6- dione 367.4 256

(2S,3R)-N,3-dihydroxy-2-({[4- (phenylethynyl)phenyl]methyl}amino)- butanamide 325.4 257

N-(3-aminopropyl)-N′-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}benzene-1,4-dicarboxamide 339.4 258

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- (propanoylamino)benzamide 310.3 259

1,1-dimethylethyl 3-[({4-[({(1S,2R)- 2-hydroxy-1-[(hydroxyamino)carbon- yl]propyl}amino)carbonyl]phenyl}- carbonyl)amino]propylcarbamate 439.5 260

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′- (phenyloxy)-1,1′-biphenyl-4- carboxamide 407.4 261

N-[(1S,2R)-1-({[cyano- (phenyl)methyl]amino}carbonyl)-2- hydroxypropyl]-4′-hydroxy-1,1′-bi- phenyl-4-carboxamide 430.5 262

4′-{[2-(hydroxyamino)-2-oxoethyl]- oxy}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 404.4 263

4′-({[(1S,2R)-1-{[(cyan- omethyl)amino]carbonyl}-2- (propanoyloxy)propyl]amino}- carbonyl)-1,1′-biphenyl-4- yl propanoate 466.5 264

4′-({[(1S,2R)-1- {[(cyanomethyl)(propanoyl)- amino]carbonyl}-2-(propanoyl- oxy)propyl]amino}carbonyl)-1,1′- biphenyl-4-yl propanoate 522.6 265

N-((1S,2R)-1-{[(cyano- methyl)amino]carbonyl}-2- hydroxypropyl)-4′-hydroxy- 1,1′-biphenyl-4-carboxamide 354.4 266

(2S,3S)-2-[(1,1′-biphenyl-4-ylmethyl)- amino]-N,3-dihydroxybutanamide 301.4 267

N-{2-hydroxy-1-[(hydroxyamino)car- bonyl]-2-phenylethyl}-1,1′-biphenyl- 4-carboxamide 377.4 268

(2S,3R)-2-[(diphenylacetyl)amino]- N,3-dihydroxybutanamide 329.4 269

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 6-[(phenylmethyl)thio]pyridine-3- carboxamide 362.4 270

N,3-dihydroxy-2-({[4- (phenyloxy)phenyl]methyl}amino)- butanamide 317.4 271

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-2′- [(trifluoromethyl)oxy]-1,1′-biphenyl-4- carboxamide 399.3 272

(2R,3S)-2-[(1,1′-biphenyl-4-ylmethyl)- amino]-N,3-dihydroxybutanamide 301.4 273

4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- amino)carbonyl]benzoic acid 283.3 274

1,1-dimethylethyl 4-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}amino)carbonyl]benzoate 339.4 275

(4R)-4-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-5-(hydroxy- amino)-5-oxopentanoic acid 371.4 276

4′-ethyl-N-[(1R)-2-(hydroxyamino)- 1-(hydroxymethyl)-2-oxoethyl]-1,1′- biphenyl-4-carboxamide 329.4 277

4′-ethyl-N-[(1S)-2-(hydroxyamino)- 1-(hydroxymethyl)-2-oxoethyl]-1,1′- biphenyl-4-carboxamide 329.4 278

(2S)-1-[(4′-ethyl-1,1′-biphenyl-4-yl)- carbonyl]-N,4-dihydroxypyrrolidine- 2-carboxamide 355.4 279

4′-ethyl-N-{(1S)-1-[(hydroxy- amino)carbonyl]but-3-ynyl}-1,1′- biphenyl-4-carboxamide 337.4 280

N-[(1S)-1-(aminomethyl)-2-(hy- droxyamino)-2-oxoethyl]-4′- ethyl-1,1′-biphenyl-4-carboxamide 328.4 281

N-{(1S)-1-[(hydroxyamino)car- bonyl]-2-methylpropyl}-1,1′-bi- phenyl-4-carboxamide 313.4 282

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- N-methyl-1,1′-biphenyl-4- carboxamide 329.4 283

4-ethynyl-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 263.3 284

4-(1,3-benzaodioxol-5-yl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 359.3 285

N-{(1R,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4′-propyl-1,1′-biphenyl-4- carboxamide 357.4 286

2-({[3′-(ethyloxy)-1,1′-biphenyl- 4-yl]methyl}amino)-N,3-dihy- droxybutanamide 345.4 287

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-3′,4′-bis(methyloxy)- 1,1′-biphenyl-4-carboxamide 375.4 288

3′-formyl-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′- (methyloxy)-1,1′-biphenyl-4- carboxamide 373.4 289

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(4-{4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- amino)carbonyl]phenyl}buta-1,3- diynyl)benzamide 523.5 290

(2S,3R)-2-({[4′-(ethyloxy)-1,1′- biphenyl-4-yl]methyl}amino)-N,3- dihydroxybutanamide 345.4 291

3′-chloro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4′- (methyloxy)-1,1′-biphenyl-4- carboxamide 379.8 292

(1R,2R)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-2- phenylcyclopropanecarboxamide 279.3 293

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(1H-pyrrol-1-yl)benzamide 304.3 294

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-propylbenzamide 281.3 295

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-pentylbenzamide 309.4 296

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-octylbenzamide 351.5 297

(2E)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 3-(4-methylphenyl)prop-2- enamide 279.3 298

(2E)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-3-[4-(trifluoromethyl)- phenyl]prop-2-enamide 333.3 299

(2E)-3-(1,1′-biphenyl-4-yl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}prop-2-enamide 341.4 300

(2S,3R)-2-[(1,1′-biphenyl-4-ylacetyl)- amino]-N,3-dihydroxybutanamide 329.4 301

(2S,3R)-2-{[(2S)-2-amino-3-(1,1′- biphenyl-4-yl)propanoyl]amino}- N,3-dihydroxybutanamide 358.4 302

(2S,3R)-2-{[(2R)-2-amino-3-(1,1′- biphenyl-4-yl)propanoyl]amino}- N,3-dihydroxybutanamide 358.4 303

(3S)-3-amino-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}-5- phenylpentanamide 310.4 304

N-{(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}- 4-[(phenylamino)methyl]- benzamide 344.4 305

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-{[(phenylmethyl)amino]methyl}- benzamide 358.4 306

4′-ethyl-N-{(1S,2R)-2-hydroxy-1- [({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}amino)carbon-yl]propyl}- 1,1′-biphenyl-4-carboxamide 444.5 307

(2S,3R)-2-[(1,1′-biphenyl-4-ylacetyl)- amino]-3-hydroxy-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbon- yl]propyl}butanamide 430.5 308

4-(4-chlorophenyl)-N-{(1S,2R)-2-- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}cyclohexane carboxamide 355.8 309

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(1H-pyrazol-1-yl)benzamide 305.3 310

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- morpholin-4-benzylamide 324.3 311

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-(1,2,3-thiadiazol-4-yl)benzamide 323.3 312

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-[(4-methylpiperazine-1-yl)- methyl]benzamide 351.4 313

N-{(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}-4- (1H-imidazol-1-ylmethyl)- benzamide 319.3 314

(2S,4S)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-phenylpyrrolidine-2-carboxamide 308.3 315

4′-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 394.2 316

4′-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 394.2 317

4′-bromo-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 394.2 318

(2R)-2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-N~1~- hydroxypentanediamide 370.4 319

(2S,3S)-1-[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]-3-hydroxypyrrolidine-2- carboxylic acid 340.4 320

(2S,3S)-N-[(1,1-dimethylethyl)oxy]- 1-[(4′-ethyl-1,1′-biphenyl-4-yl)- carbonyl]-3-hydroxypyrrolidine-2- carboxamide 411.5 321

(2S,3S)-1-[(4′-ethyl-1,1′-biphenyl- 4-yl)carbonyl]-N,3-dihydroxy- pyrrolidine-2-carboxamide 355.4 322

N-{(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}-4-[(4- nitrophenyl)ethynyl]benzamide 384.4 323

N-{(1S,2R)-2-hydroxy-1-[(hy droxyamino)carbonyl]propyl}-4-{[4- (1H-pyrrol-1-yl)phenyl]ethylnyl}- benzamide 404.4 324

N-{(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}- 4′-nitro-1,1′-biphenyl-4-car- boxamide 360.3 325

(2S,3R)-N,3-dihydroxy-2-({[4′-(meth- yloxy)-3′-propyl-1,1′-biphenyl-4- yl]methyl}amino)butanamide 373.5 326

4′-cyano-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 1,1′-biphenyl-4-carboxamide 340.3 327

(2S,3R)-2-({[4′-(ethyloxy)-4-(methyl- oxy)-1,1′-biphenyl-3-yl]methyl}- amino)-N,3-dihydroxybutanamide 375.4 328

2′,5′-difluoro-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-1,1′- biphenyl-4-carboxamide 351.3 329

N-[(1S)-1-[(acetylamino)methyl]-2- (hydroxyamino)-2-oxoethyl]-4′-ethyl- 1,1′-biphenyl-4-carboxamide 370.4 330

N-{(1S)-4-amino-1- [(hydroxyamino)carbonyl]butyl}-4′- ethyl-1,1′-biphenyl-4-carboxamide 356.4 331

4′-ethyl-N-[(1S)-2-(hydroxyamino)-1- (1H-imidazol-5-ylmethyl)-2-oxo- ethyl]-1,1′-biphenyl-4-carboxamide 379.4 332

(2S,3R)-2-{[1-(1,1′-biphenyl-4- yl)ethyl]amino}-N,3-dihydroxy- butanamide 315.4 333

(2S,3R)-2-{[1-(1,1′-biphenyl-4- yl)propyl]amino}-N,3-dihydroxy- butanamide 329.4 334

(2S,3R)-2-{[1-(4′-bromo-1,1′-bi- phenyl-4-yl)ethyl]amino}-N,3- dihydroxybutanamide 394.3 335

(2S,3R)-N,3-dihydroxy-2-{[1-(4′-methyl- 1,1′-biphenyl-4-yl)ethyl]amino}- butanamide 329.4 336

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-1,1′-biphenyl-4- carboxamide 300.3 337

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-(1H-pyrrol-1- yl)benzamide 289.3 338

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-(4- chlorophenyl)cyclohexane- carboxamide 340.8 339

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-pentylbenzamide 294.4 340

(2E)-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]-3-(1,1′- biphenyl-4-yl)prop-2-enamide 326.4 341

(2S)-3-amino-2-{[(4′-ethyl-1,1′-bi- phenyl-4-yl)methyl]amino}-N- hydroxypropanamide 314.4 342

(2S)-3-amino-2-[(1,1′-biphenyl-4- ylmethyl)amino]-N-hydroxy- propanamide 286.3 343

(2S)-3-amino-2-{[1-(4′-bromo-1,1′- biphenyl-4-yl)ethyl]amino}-N- hydroxypropanamide 379.3 344

(2S)-3-amino-N-hydroxy-2-{[1- (4′-methyl-1,1′-biphenyl-4-yl)ethyl]amino}propanamide 314.4 345

4′-ethyl-N-[(1S)-2-({(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}amino)-1- (hydroxymethyl)-2-oxoethyl]- 1,1′-biphenyl-4-carboxamide 430.5 346

4′-ethyl-N-{(1S)-2-({(1S,2R)-2-hy- droxy-1-[(hydroxyamino)carbonyl]- propyl}amino)-1-[(4-hydroxy- phenyl)methyl]-2-oxoethyl}-1,1′- biphenyl-4-carboxamide 506.6 347

(2S)-2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-N~1~-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}pentanediamide 471.5 348

(4S)-4-{[(4′-ethyl-1,1′-biphenyl-4-yl)- carbonyl]amino}-5-({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)-5- oxopentanoic acid 472.5 349

(3S)-3-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-4-({(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}amino)-4-oxobutanoic acid 458.5 350

(3S)-2-(1,1′-biphenyl-4-ylacetyl)- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-1,2,3,4-tetrahydroiso- quinoline-3-carboxamide 488.6 351

4′-ethyl-N-[(1S)-2-({(1S,2R)-2- hydroxy-1-[(hydroxyamino)car- bonyl]propyl}amino)-1-methyl- 2-oxoethyl]-1,1′-biphenyl-4- carboxamide 414.5 352

(2S,3R)-2-({(2S)-3-amino-2-[(1,1′- biphenyl-4-ylacetyl)amino]pro- panoyl}amino)-N,3- dihydroxybutanamide 415.5 353

(2S)-2-[(1,1′-biphenyl-4-ylacetyl)- amino]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- pent-4-ynamide 424.5 354

(2S,3R)-2-{[(2S)-2-amino-2-(1,1′- biphenyl-4-yl)ethanoyl]amino}-N,3- dihydroxybutanamide 344.4 355

(2S,3R)-2-{[(2R)-2-amino-2-(1,1′- biphenyl-4-yl)ethanoyl]amino}-N,3- dihydroxybutanamide 344.4 356

N-(3-aminopropyl)-4′-ethyl-N-[2- (hydroxyamino)-2-oxoethyl]- 1,1′-biphenyl-4-carboxamide 356.4 357

N-(2-cyanoethyl)-4′-ethyl-N-[2- (hydroxyamino)-2-oxoethyl]-1,1′- biphenyl-4-carboxamide 352.4 358

N-[2-(acetylamino)ethyl]-4′-ethyl- N-[2-(hydroxyamino)-2-oxoethyl]- 1,1′-biphenyl-4-carboxamide 384.4 359

4′-ethyl-N-[2-(hydroxyamino)-2-oxo- ethyl]-N-prop-2-ynyl-1,1′-biphenyl- 4-carboxamide 337.4 360

4-cyano-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 264.3 361

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-cyanobenzamide 249.2 362

1,1-dimethylethyl (2S)-2-{[(4- ethynylphenyl)carbonyl]amino}-3- (hydroxyamino)-3- oxopropylcarbamate 348.4 363

1,1-dimethylethyl (2S)-3-(hydroxyamino)- 3-oxo-2-[({4-[(E)-2- phenylethenyl]phenyl}methyl)- amino]propylcarbamate 412.5 364

N-{(1R,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 3′-(trifluoromethyl)-1,1′-biphenyl- 4-carboxamide 383.3 365

(2S,3R)-2-[(1,1′-biphenyl-4-yl- methyl)amino]-3-hydroxy- butanoic acid 286.3 366

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-(phenylethynyl)- benzamide 324.4 367

1,1-dimethylethyl (2S)-3-(hydroxy- amino)-3-oxo-2-({[4-(phenylethynyl)- phenyl]carbonyl}amino)propyl- carbamate 424.5 368

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-ethynyl- benzamide 248.3 369

N-[(1S)-1-(aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]-4-ethynyl-0 benzamide 248.3 370

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4- {[4-(methyloxy)phenyl]ethynyl}- benzamide 369.4 371

(2S)-3-amino-N-hydroxy-2-[({4- [(E)-2-phenylethenyl]phenyl}- methyl)amino]proanamide 312.4 372

1,1-dimethylethyl-2-{4′-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}amino)carbon-yl]-1,1′-biphenyl- 4-yl}ethylcarbamate 458.5 373

(2S,3R)-N,3-dihydroxy-2-[({4′-[(2-pyrrolidin- 1-ylethyl)oxy]-1,1′-biphenyl-4- yl}methyl)amino]butanamide 414.5 374

1,1-dimethylethyl (1S)-4-({[(1,1- dimethylethyl)oxy]carbonyl}amino)-1-({[4- ({4-[({(1S,2R)-2-hydroxy-1- [hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]amino}carbonyl)- butylcarbamate 668.8 375

4-(4-chlorophenyl)-N-[(1S)-2-({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)-1- methyl-2-oxoethyl]cyclohexanecarboxamide 426.9 376

4′-ethyl-N-[2-({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)-2- oxoethyl]-1,1′-biphenyl-4-carboxamide 400.4 377

4′-ethyl-N-[3-({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)-3- oxopropyl]-1,1′-biphenyl-4-carboxamide 414.5 378

4′-ethyl-N-[4-({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)-4- oxobutyl]-1,1′-biphenyl-4-carboxamide 428.5 379

N-((1S)-2-{[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]amino}-1-methyl- 2-oxoethyl)-4′-ethyl-1,1′-biphenyl-4- carboxamide 399.5 380

N-(2-{[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]amino}-2- oxoethyl)-4′-ethyl-1,1′-biphenyl-4- carboxamide 385.4 381

N-(3-{[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]amino}-3- oxopropyl)-4′-ethyl-1,1′-biphenyl-4- carboxamide 399.5 382

N-(4-{[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]amino}-4- oxobutyl)-4′-ethyl-1,1′-biphenyl-4- carboxamide 413.5 383

4′-ethyl-N-[1-(hydroxyamino)carbonyl]-2- (methyloxy)propyl]-1,1′-biphenyl-4- carboxamide 357.4 384

4′-ethyl-N-[(1S,2R)-1- [(hydroxyamino)carbonyl]-2- (methyloxy)propyl]-1,1′-biphenyl- 4-carboxamide 357.4 385

N-[1-[(dimethylamino)methyl]-2- (hydroxyamino)-2-oxoethyl]-4′- ethyl-1,1′-biphenyl-4- carboxamide 356.4 386

N-{(1S)-3-cyano-1-[(hydroxy- amino)carbonyl]propyl}-4′- ethyl-1,1′-biphenyl-4-car- boxamide 352.4 387

N-{(1S)-5-amino-1-[(hydroxy- amino)carbonyl]pentyl}-4′- ethyl-1,1′-biphenyl-4- carboxamide 370.5 388

N-{(1S)-3-amino-1- [(hydroxyamino)car- bonyl]propyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 342.4 389

4′-ethyl-N-hydroxy-1,1′- biphenyl-4-carboxamide 242.3 390

4′-ethyl-N-{2-hydroxy-1- [(hydroxyamino)carbonyl]-2-methylpropyl}- 1,1′-biphenyl-4-carboxamide 357.4 391

N-[(2S)-2-{[(4′-ethyl-1,1′-bi- phenyl-4-yl)carbonyl]amino}- 3-(hydroxyamino)-3-oxo- propyl]morpholine-4- carboxamide 441.5 392

N-[(1S)-1-{[(amino- carbonyl)amino]methyl}-2- (hydroxyamino)-2-oxoethyl]-4′- ethyl-1,1′-biphenyl-4- carboxamide 371.4 393

N-[(1S)-1-({[amino(imino)- methyl]amino}mthyl)-2- (hydroxyamino)-2-oxo- ethyl]-4′-ethyl-1,1′- biphenyl-4-carboxamide 370.4 394

N-[(2S)-2-amino-3-(hydroxy- amino)-3-oxopropyl]-4′-ethyl- 1,1′-biphenyl-4-carboxamide 328.4 395

1-[(4′-ethyl-1,1′-biphenyl-4-yl)- carbonyl]-N-hydroxypiperazine- 2-carboxamide 354.4 396

N-[(2S)-2-amino-3-(hydroxy- amino)-3-oxopropyl]-4- (phenylethynyl)benzamide 324.4 397

N-hydroxy-1-{[4-(phenyl- ethynyl)phenyl]carbonyl}- piperazine-2-carboxamide 350.4 398

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-pentylphenyl)- ethynyl]benzamide 409.5 399

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[3-(methyloxy)- phenyl]ethynyl}benzamide 369.4 400

4-[(3-fluoro-4-methylphenyl)- ethynyl]-N-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 371.4 401

4-[(2,4-difluorophenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 375.3 402

methyl (2E)-3-(ethylamino)-2- ({[4-(phenylethynyl)phenyl]- carbonyl}amino)but-2-enoate 363.4 403

1,1-dimethylethyl 4-{[(2S)-3- (hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]- carbonyl}amino)propyl]- amino}-4-oxobutylcarbamate 509.6 404

N-(1-(N-hydroxycarbamoyl)- 2-hydroxy-3-methylbutyl)- [4-(4-ethylphenyl)phenyl]- carboxamide 371.4 405

N-((1R,2R)-1-{[(aminocar- bonyl)(hydroxy)amino]- methyl}-2-hydroxypropyl)- 4′-ethyl-1,1′-biphenyl-4- carboxamide 372.4 406

4′-ethyl-N-((1R,2R)-1- {[formyl(hydroxy)amino]- methyl}-2-hydroxypropyl)- 1,1′-biphenyl-4-carboxamide 357.4 407

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-(trifluoromethyl)- phenyl]ethynyl}benzamide 407.4 408

1,1-dimethylethyl 2-{[(2S)-3- (hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]- carbonyl}amino)propyl]- amino}-2-oxoethylcarbamate 481.5 409

N-[(1S)-1-{[(aminoacetyl)- amino]methyl}-2- (hydroxyamino)-2-oxoethyl]- 4-(phenylethynyl)benzamide 381.4 410

N-[(1S)-1-{[(4-aminobutanoyl)amino]methyl}- 2-(hydroxyamino)-2-oxoethyl]- 4-(phenylethynyl)benzamide 409.5 411

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-pent-1- ynylbenzamide 305.3 412

N-{(1S,2R)-2-[(1,1-dimethyl- ethyl)oxy]-1-[(hydroxyamino)car- bonyl]propyl}-4′-propyl- 1,1′-biphenyl-4-carboxamide 413.5 413

1,1-dimethylethyl (1S)-4-({[(1,1- dimethylethyl)oxy]carbonyl}- amino)-1-{[(2-{4′-[({(1S,2R)- 2-hydroxy-1-[(hydroxyamino)car- bonyl]propyl}amino)carbon- yl]-1,1′-biphenyl-4-yl}ethyl)- amino]carbonyl}butylcarbamate 672.8 414

4′-(2-aminoethyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}-1,1′- biphenyl-4-carboxamide 358.4 415

4′-(2-{[(2S)-2,5-diamino- pentanoyl]amino}ethyl)-N- {(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]- propyl}-1,1′-biphenyl-4- carboxamide 472.6 416

4-(cyclohex-1-en-1-ylethynyl)- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 343.4 417

4-(3,3-dimethylbut-1-ynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 319.4 418

N-{(1S)-1-{[(aminoacetyl)amino]- methyl}-2-[(2-{[(2S)-3-(hydroxy- amino)-3-oxo-2-({[4-(phenyl- ethynyl)phenyl]carbonyl}- amino)propyl]-amino}-2- oxoethyl)amino]-2-oxoethyl}-4- (phenylethynyl)benzamide 728.8 419

4-[(4-{[(2S)-2,5-diamin- opentanoyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 468.5 420

4′-(2-aminoethyl)-N-{(1E)-1- [(hydroxyamino)carbonyl]prop- 1-enyl}-1,1′-biphenyl- 4-carboxamide 340.4 421

2′,4′-difluoro-N-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)car- bonyl]propyl}-1,1′- biphenyl-4-carboxamide 351.3 422

N-[(1E)-1-formylprop-1-enyl]- 4′-propyl-1,1′-biphenyl- 4-carboxamide 308.4 423

N-hydroxy-4-(pyridin-3-ylethynyl)benzamide 239.2 424

4-(3-hydroxy-3,5-dimethylhex- 1-ynyl)-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 363.4 425

4′-ethyl-N-{(1R,2R)-2-hydroxy-1- [(hydroxyamino)methyl]propyl}- 1,1′-biphenyl-4-carboxamide 329.4 426

4′-ethyl-N-{(1R,2R)-1- [(hydroxyamino)methyl]-2- [(phenylmethyl)oxo]propyl}-1,1′- biphenyl-4-carboxamide 419.5 427

4′-ethyl-N-[(5R,6R)-3-hydroxy- 6-methyl-2-oxo-1,3-oxazinan- 5-yl]-1,1′-biphenyl-4-car- boxamide 355.4 428

N-((1R,2R)-1-{[({[2-(di- methylamino)ethyl]amino}- carbonyl)(hydroxy)amino]- methyl}-2-hydroxypropyl)-4′- ethyl-1,1′-biphenyl-4-car- boxamide 443.6 429

N-((1R,2R)-1-{[{[(2-cyano- ethyl)amino]carbonyl}(hydroxy)- amino]methyl}-2-hydroxypropyl)- 4′-ethyl-1,1′-biphenyl-4- carboxamide 425.5 430

4′-ethyl-N-((1R,2R)-2-hydroxy-1- {[hydroxy({[3-(2-oxopyrrolidin-1- yl)propyl]amino}carbonyl)amino]- methyl}prop-yl)-1,1′-biphenyl-4- carboxamide 497.6 431

(1R,2R)-3-[({[2-(dimethyl- amino)ethyl]amino}carbonyl)- (hydroxy)amino]-2-{[(4′-ethyl- 1,1′-biphenyl-4-yl)carbonyl]- amino}-1-methylpropyl 2- (dimethylamino)ethylcarbamate 557.7 432

(1R,2R)-3-[{[(2-cyanoethyl)- amino]carbonyl}(hydroxy)amino]- 2-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-1-methyl- propyl 2-cyanoethylcarbamate 521.6 433

N-{(1E)-1-[(E)-(hydroxyimino)- methyl]prop-1-enyl}-4′-propyl- 1,1′-biphenyl-4-carboxamide 323.4 434

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-(pyridin-3- ylethynyl)benzamide 340.3 435

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[3-(methylamino)- prop-1-ynyl]benzamide 306.3 436

N-[(1S)-1-[(dimethylamino)- methyl]-2-(hydroxyamino)-2- oxoethyl]-4′-ethyl-1,1′- biphenyl-4-carboxamide 356.4 437

N-[1-(N-hydroxycarba- moylmethyl)(1R,2R)-2- hydroxypropyl][4-(4- ethylphenyl)phenyl]carboxamide 357.4 438

N-[(1S)-1-[(diethylamino)- methyl]-2-(hydroxyamino)-2- oxoethyl]-4′-ethyl-1,1′- biphenyl-4-carboxamide 384.5 439

4-[(3-aminophenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 354.4 440

4-[3-(dimethylamino)prop-1- ynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 320.4 441

4-[3-(dimethylamino)prop-1- ynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 320.4 442

4-({4-[(aminoacetyl)amino]- phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 411.4 443

3′-fluoro-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}-4′-methyl- 1,1′-biphenyl-4-carboxamide 347.4 444

N-[(1S)-1-formyl-2-methyl- propyl]-1,1′-biphenyl-4- carboxamide 282.4 445

N-{(1S)-1-[(E)-(hydroxyamino)- methyl]-2-methylpropyl}-1,1′- biphenyl-4-carboxamide 297.4 446

N-((1E)-1-{(E)-[(amino- carbonyl)hydrazono]methyl}- prop-1-enyl)-4′-propyl-1,1′- biphenyl-4-carboxamide 365.4 447

4-[(4-aminophenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 354.4 448

4-{[3-(aminomethyl)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 368.4 449

N-(2-aminoethyl)-3-({4- [({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}amino)carbnyl]- phenyl}ethynyl)benzamide 425.5 450

N-((1S)-1-{(E)-[(amino- carbonyl)hydrazono]methyl}-2- methylpropyl)-1,1′-biphenyl-4- carboxamide 339.4 451

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[3-(propanoylamino)- phenyl]ethynyl}benzamide 410.4 452

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[3-(morpholin-4- ylmethyl)phenyl]ethynyl}- benzamide 438.5 453

4-[(3-{[(2-aminoethyl)- amino]methyl}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 411.5 454

N-[(1R)-2-(hydroxyamino)-1- (hydroxymethyl)-2-oxo- ethyl]-4′-propyl-1,1′-biphenyl-4- carboxamide 343.4 455

N-[1-(N-hydroxycar- bamoylmethyl)(1R,2R)-2- hydroxypropyl][4-(2- phenylethynyl)phenyl]- carboxamide 353.4 456

4′-ethyl-N-[(1R,2R)-1- [(hydroxyamino)carbonyl]-2- (methyloxy)propyl]-1,1′- biphenyl-4-carboxamide 357.4 457

4′-ethyl-N-[(1S)-1-[(ethyl- amino)methyl]-2- (hydroxyamino)-2-oxo- ethyl]-1,1′-biphenyl-4- carboxamide 356.4 458

4′-ethyl-N-[(1S)-2-(hydroxy- amino)-2-oxo-1- ({[(2S)-pyrrolidin-2- ylmethyl]amino}methyl)- ethyl]-1,1′-biphenyl-4- carboxamide 411.5 459

N-[(1S)-1-[(ethylamino)methyl]- 2-(hydroxyamino)-2-oxoethyl]- 4-(phenylethynyl)benzamide 352.4 460

N-[(1S)-2-(hydroxyamino)-2- oxo-1-({[(2S)-pyrrolidin-2- ylmethyl]amino}methyl)- ethyl]-4-(phenylethynyl)- benzamide 407.5 461

4′-ethyl-N-((1S)-2-(hydroxy- amino)-1-{[(1-methylethyl)amino]- methyl}-2-oxoethyl)-1,1′- biphenyl-4-carboxamide 370.5 462

4′-ethyl-N-[(1S)-2-(hydroxy- amino)-1-({[2-(methyl- amino)ethyl]amino}methyl)-2- oxoethyl]-1,1′-biphenyl-4-car- boxamide 385.5 463

4′-ethyl-N-((1S)-2-(hydroxy- amino)-1-{[(1-methyl- piperidin-4-yl)amino]methyl}- 2-oxoethyl)-1,1′-biphenyl-4- carboxamide 425.5 464

N-((1S)-2-(hydroxyamino)-1- {[(1-methylethyl)amino]- methyl}-2-oxoethyl)-4- (phenylethynyl)benzamide 366.4 465

N-[(1S)-2-(hydroxyamino)-1- ({[2-(methylamino)ethyl]amino}- methyl)-2-oxoethyl]-4- (phenylethynyl)benzamide 381.4 466

N-((1S)-2-(hydroxyamino)-1- {[(1-methylpiperidin-4-yl)- amino]methyl}-2-oxo- ethyl)-4-(phenylethynyl)- benzamide 421.5 467

N-[(1S)-1-{[(2-aminoethyl)amino]- methyl}-2-(hydroxyamino)-2- oxoethyl]-4-(phenylethynyl)- benzamide 367.4 468

N-[(1S)-1-{[bis(2-aminoethyl)- amino]methyl}- 2-(hydroxyamino)-2-oxoethyl]-4- (phenylethynyl)benzamide 410.5 469

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(morpholin- 4-ylacetyl)amino]phenyl}- ethynyl)benzamide 481.5 470

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-(propanoylamino)- phenyl]ethynyl}benzamide 410.4 471

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(trifluoromethyl)- oxy]phenyl}ethynyl)benzamide 423.4 472

1,1-dimethylethyl (2S)-3-(hy- droxyamino)-3-oxo-2-{[(4- {[3-(propanoylamino)phenyl]- ethynyl}phenyl)car- bonyl]amino}propylcarbamate 495.5 473

1,1-dimethylethyl (2S)-3- (hydroxyamino)-3- oxo-2-{[(4-pent-1- ynylphenyl)carbonyl]- amino}propylcarbamate 390.4 474

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[3-(pro- panoylamino)phenyl]- ethynyl}benzamide 395.4 475

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-pent-1- ynylbenzamide 290.3 476

4-(phenyloxy)benzaldehyde thiosemicarbazone 272.3 477

4-(phenyloxy)benzaldehyde semicarbazone 256.3 478

4-{[3-(trifluoromethyl)- phenyl]oxy}benzaldehyde thiosemicarbazone 340.3 479

4-[(3,4-difluorophenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 375.3 480

4-[(2,4-dioxo-1,2,3,4- tetrahydropyrimidin-5- yl)ethynyl]-N-{(1S,2R)-2- hydroxy-1-[(hydroxy- amino)carbonyl]-propyl} benzamide 373.3 481

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-(4-phenylbuta-1,3- diynyl)benzamide 348.4 482

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4′-propyl-1,1′-biphenyl- 4-carboxamide 342.4 483

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-1,1′:4′,1″-terphenyl- 4-carboxamide 376.4 484

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-1,1′:4′,1″- terphenyl-4-carboxamide 391.4 485

1,1-dimethylethyl (2S)-2-[({4- [(4-{[({[(1,1-dimethylethyl)- oxy]carbonyl}amino)acetyl]- amino}phenyl)ethynyl]phenyl}- carbonyl)amino]-3- (hydroxyamino)-3-oxo- propylcarbamate 596.6 486

N-[(1S,2R)-1-(hydrazinocar- bonyl)-2-hydroxypropyl]-4- (phenylethynyl)benzamide 338.4 487

2-[(2S,3R)-3-hydroxy-2-({[4- (phenylethynyl)phenyl]car- bonyl}amino)butanoyl]- hydrazinecarboxamide 381.4 488

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(2-methyl- phenyl)ethynyl]benzamide 353.4 489

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(3-hydroxy- phenyl)ethynyl]benzamide 355.4 490

4-({3-[(aminoacetyl)amino]- phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 411.4 491

4-{[4-({[(cyanomethyl)- amino]acetyl}amino)phenyl] ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 450.5 492

4′-ethyl-N-{(1S)-2-(hydroxy- amino)-2-oxo-1-[(tetrahydro- 2H-pyran-4-ylamino)methyl]- ethyl}-1,1′-biphenyl-4- carboxamide 412.5 493

N-{(1S)-2-(hydroxyamino)-2- oxo-1-[(tetrahydro-2H-pyran- 4-ylamino)methyl]ethyl}-4- (phenylethynyl)benzamide 408.5 494

4-[(4-chlorophenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 373.8 495

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-methyl- phenyl)ethynyl]benzamide 353.4 496

4-[(2-fluorophenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 357.4 497

4-[(3-fluorophenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 357.4 498

4-[(4-fluorophenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 357.4 499

4-[(4-{[(cyclopropylamino)- acetyl]amino}phenyl-ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 451.5 500

4-({4-[({[2-(dimethylamino)- ethyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 482.6 501

4-({4-[({[2-(acetylamino)- ethyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 496.5 502

N-{(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}- 4-({4-[({[3-(2-oxopyrrolidin- 1-yl)propyl]amino}acetyl)- amino]phenyl}ethynyl)- benzamide 536.6 503

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(pyridin-3- ylmethyl)amino]acetyl}- amino)phenyl]ethynyl} benzamide 502.5 504

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2-pyridin- 2-ylethyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 516.6 505

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-[(4-{[(4-methylpiperazin-1- yl)acetyl]amino}phenyl)- ethynyl]benzamide 494.6 506

4-({4-[(1,4′-bipiperidin-1′- ylacetyl)amino]phenyl}ethynyl)- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 562.7 507

1-(2-{[4-({4-[({(1S,2R)-2- hydroxy-1-[(hydroxyamino)car- bonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]- amino}-2-oxoethyl)piperidine- 4-carboxamide 522.6 508

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{(piperidin-3- ylamino)acetyl]amino}phenyl)- ethynyl]benzamide 494.6 509

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(piperidin-4- ylamino)acetyl]amino}- phenyl)ethynyl]benzamide 494.6 510

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(piperidin- 2-ylmethyl)amino]acetyl}- amino)phenyl]ethynyl} benzamide 508.6 511

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(piperidin- 3-ylmethyl)amino]acetyl}- amino)phenyl]ethynyl} benzamide 508.6 512

4-[(4-{[(3-aminopyrrolidin- 1-yl)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hy- droxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 480.5 513

4-({4-[(azepan-1-ylacetyl)- amino]phenyl}ethynyl)- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 493.6 514

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(4- morpholin-4-ylphenyl)amino]- acetyl}amino)phenyl]ethynyl}- benzamide 572.6 515

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- hydroxyethyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 440.5 516

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-[(4-{[(cyclopropylamino)- acetyl]amino}phenyl)- ethynyl]benzamide 436.5 517

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxo- ethyl]-4-({4-[({[3-(2-oxo- pyrrolidin-1-yl)propyl]amino}- acetyl)amino]phenyl}ethynyl)- benzamide 521.6 518

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxo- ethyl]-4-[(4-{[(4-methyl- piperiazin-1-yl)acetyl]amino}- phenyl)ethynyl]benzamide 479.6 519

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxo- ethyl]-4-{[4-({[(pyridin-3- ylmethyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 487.5 520

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[(piperidin- 1-ylacetyl)amino]phenyl}- ethynyl)benzamide 464.5 521

4-{[4-({[(2-hydroxy- ethyl)amino]acetyl}amino)- phenyl]-ethynyl}-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 455.5 522

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({[2-(methyl- oxy)ethyl]amino}acetyl)- amino]phenyl}- ethynyl)benzamide 469.5 523

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({methyl[2- (methyloxy)ethyl]amino}- acetyl)amino]phenyl}- ethynyl)benzamide 483.5 524

4-{[4-({[[2-(dimethyl- amino)ethyl](methyl)amino]- acetyl}-amino)phenyl]- ethynyl}-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 496.6 525

4-{[4-({[(3R)-3-(dimethyl- amino)pyrrolidin-1-yl]- acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 508.6 526

4-{[4-({[(3S)-3-(dimethyl- amino)pyrrolidin-1-yl]acetyl}- amino)phenyl]ethynyl}-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 508.6 527

4-{[4-({[(3R)-3-(acetylamino)- pyrrolidin-1-yl]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 522.6 528

4-{[4-({[(3S)-3-(acetylamino)- pyrrolidin-1-yl]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 522.6 529

4-{[4-({[(3R)-1-azabi- cyclo[2.2.2]oct-3-ylamino]- acetyl}amino)phenyl]ethynyl}- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 520.6 530

4-{[4-({[(3S)-1-azabi- cyclo[2.2.2]oct-3-ylamino]- acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 520.6 531

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({[(2R)- pyrrolidin-2-ylmethyl]amino}- acetyl)amino]phenyl}ethynyl) benzamide 494.6 532

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({[(2S)- pyrrolidin-2-ylmethyl]amino}- acetyl)amino]phenyl}ethynyl) benzamide 494.6 533

4-{[4-({[(3-aminocyclo- hexyl)amino]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 508.6 534

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(3-hydroxy- piperidin-1-yl)acetyl]amino}- phenyl)ethynyl]benzamide 495.5 535

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(3-mor- pholin-4-ylpropyl)amino]- acetyl}amino)phenyl]- ethynyl}benzamide 538.6 536

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2-methyl- propyl)amino]acetyl}amino)- phenyl]-ethynyl}benzamide 467.5 537

4-[(4-{[(ethylamino)- acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 439.5 538

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(piperidin-1- ylacetyl)amino]phenyl}- ethynyl)benzamide 479.5 539

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(3-hydroxy- propyl)amino]acetyl}amino)- phenyl]-ethynyl}benzamide 469.5 540

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({[3- (methyloxy)propyl]amino}- acetyl)amino]phenyl}- ethynyl)benzamide 483.5 541

4-{[4-({[(2- cyanoethyl)amino]acetyl}- amino)phenyl]ethynyl}- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 464.5 542

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2- pyrrolidin-1-ylethyl)amino]- acetyl}amino)phenyl]ethynyl}- benzamide 508.6 543

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(2- methyl-1H-imidazol-1- yl)acetyl]amino}phenyl)- ethynyl]benzamide 476.5 544

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4- {[(methylamino)acetyl]amino}- phenyl)ethynyl]benzamide 410.4 545

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- methylpropyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 452.5 546

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({[2- (methyloxy)ethyl]amino}- acetyl)amino]phenyl}- ethynyl)benzamide 454.5 547

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({methyl[2- (methyloxy)ethyl]amino}- acetyl)amino]phenyl}- ethynyl)benzamide 468.5 548

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(3- hydroxypropyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 454.5 549

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({[3- (methyloxy)propyl]amino}- acetyl)amino]phenyl}- ethynyl)benzamide 468.5 550

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({[2- (dimethylamino)ethyl]- amino}acetyl)amino]- phenyl}ethynyl)benzamide 467.5 551

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[[2- (dimethylamino)ethyl]- (methyl)amino]acetyl}- amino)phenyl]ethynyl}benzamide 481.6 552

4-({4-[({[2- (acetylamino)ethyl]amino}- acetyl)amino]phenyl}- ethynyl)-N-[(1S)-1-(amino- methyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 481.5 553

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- cyanoethyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 449.5 554

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2-pyrrolidin- 1-ylethyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 493.6 555

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({[4- (dimethylamino)butyl]amino}- acetyl)amino]- phenyl}ethynyl)benzamide 495.6 556

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[(morpholin-4- ylacetyl)amino]phenyl}- ethynyl)benzamide 466.5 557

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[(azepan-1- ylacetyl)amino]phenyl}- ethynyl)benzamide 478.6 558

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[(pyrrolidin-1- ylacetyl)amino]phenyl}- ethynyl)benzamide 450.5 559

1-{2-[(4-{[4-({[(1S)-1- (aminomethyl)-2-(hydroxy- amino)-2-oxoethyl]amino}car- bonyl)phenyl]ethynyl}- phenyl)amino]-2-oxoethyl}- piperidine-4-carboxamide 507.6 560

4-{[4-({[(3R)-3-(acetylamino)- pyrrolidin-1-yl]acetyl}amino)- phenyl]ethynyl}-N-[(1S)-1- (aminomethyl)-2-(hydroxyamino)- 2-oxoethyl]benzamide 507.6 561

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(3R)-3- (dimethylamino)pyrrolidin-1- yl]acetyl}amino)phenyl]ethynyl}- benzamide 493.6 562

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4-{[(3-amino- pyrrolidin-1-yl)acetyl]amino}- phenyl)ethynyl]benzamide 465.5 563

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4-{[(piperidin-3- ylamino)acetyl]amino}phenyl)- ethynyl]-benzamide 479.6 564

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4-{[(piperidin-4- ylamino)acetyl]amino}phenyl)- ethynyl]benzamide 479.6 565

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(piperidin-2- ylmethyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 493.6 566

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(piperidin- 3-ylmethyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 493.6 567

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(pyridin-2- ylmethyl)amino]acetyl}amino)- phenyl]ethynyl} benzamide 487.5 568

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(pyridin-4- ylmethyl)amino]acetyl}amino)- phenyl]ethynyl} benzamide 487.5 569

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2-pyridin-2- ylethyl)amino]acetyl}amino)- phenyl]ethynyl}- benzamide 501.6 570

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2-pyridin-3- ylethyl)amino]acetyl}amino)- phenyl]ethynyl}- benzamide 501.6 571

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2-pyridin-4- ylethyl)amino]acetyl}amino)- phenyl]ethynyl}- benzamide 501.6 572

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4- {[(phenylamino)acetyl]amino}- phenyl)ethynyl] benzamide 472.5 573

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4- ({[(phenylmethyl)amino]acetyl}- amino)phenyl] ethynyl}benzamide 486.5 574

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- phenylethyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 500.6 575

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[(1H-imidazol-1- ylacetyl)amino]phenyl}ethynyl)- benzamide 447.5 576

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(1H- imidazol-1-ylacetyl)amino]- phenyl}ethynyl)benzamide 462.5 577

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(phenylamino)- acetyl]amino}phenyl)ethynyl]- benzamide 487.5 578

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2- phenylethyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 515.6 579

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(3-phenyl- propyl)amino]acetyl}amino)- phenyl]-ethynyl}benzamide 529.6 580

4-[(3- {[(aminoacetyl)amino]methyl}- phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 425.5 581

4-[(2-aminopyrimidin-5-yl)- ethynyl]-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 356.4 582

4-[(4-acetylphenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 381.4 583

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[({2-[4- (phenylmethyl)piperiazin-1- yl]ethyl}amino)acetyl]amino}- phenyl)ethynyl]benzamide 613.7 584

4-{[4-({[(aminoacetyl)amino]- acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 468.5 585

4-{[4-({[4-(2-hydroxyethyl)- piperiazin-1-yl]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 524.6 586

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({(3R)-3- [(trifluoroacetyl)amino]- pyrrolidin-1-yl}acetyl)amino]- phenyl}ethynyl)benzamide 576.5 587

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(methylamino)- acetyl]amino}phenyl)ethynyl] benzamide 425.5 588

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(piperazin-1- ylacetyl)amino]phenyl}- ethynyl)benzamide 480.5 589

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(pyridin-2- ylmethyl)amino]acetyl}- amino)phenyl]ethynyl} benzamide 502.5 590

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(pyridin-4- ylmethyl)amino]acetyl}- amino)phenyl]ethynyl} benzamide 502.5 591

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2-pyridin- 3-ylethyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 516.6 592

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2-pyridin- 4-ylethyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 516.6 593

4-({4-[({[(2-fluorophenyl)- methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 519.5 594

4-({4-[({[(2-chlorophenyl)- methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)car- bonyl]propyl}benzamide 536.0 595

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[({[2- (methyloxy)phenyl]methyl}- amino)acetyl]-amino}phenyl)- ethynyl]benzamide 531.6 596

4-({4-[({[(3-fluorophenyl)- methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 519.5 597

4-({4-[({[(3-chlorophenyl)- methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 536.0 598

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[({[3- (methyloxy)phenyl]methyl}- amino)acetyl]amino}- phenyl)ethynyl]benzamide 531.6 599

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({[(3-methyl- phenyl)methyl]amino}- acetyl)amino]phenyl}- ethynyl)benzamide 515.6 600

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[({[3- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 569.5 601

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[({3- [(trifluoromethyl)oxy]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 585.5 602

4-({4-[({[(4- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 519.5 603

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[(4- methylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 515.6 604

4-[(4-{[({[4- (dimethylamino)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]propyl}benzamide 544.6 605

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[({[4- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 569.5 606

4-[(4-{[({[4-fluoro-2- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]propyl}benzamide 587.5 607

4-({4-[({[(2,4- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 537.5 608

4-({4-[({[(2,4- dichlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 570.4 609

4-{[4-({[(2- fluorophenyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 505.5 610

4-{[4-({[(4-fluorophenyl)amino]- acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 505.5 611

4-({4-[({[(3,5- difluorophenyl)- methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl} benzamide 537.5 612

4-{[4-({[(4-bromophenyl)- amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 566.4 613

4-({4-[({[4- (dimethylamino)phenyl]-amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 530.6 614

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4-{[(2S)-2- aminopropanoyl]amino}- phenyl)ethynyl]-benzamide 410.4 615

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2R)-2- aminopropanoyl]amino}- phenyl)ethynyl]- benzamide 410.4 616

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2S)-2- amino-4-methylpentanoyl]- amino}phenyl)ethynyl]- benzamide 452.5 617

4-[(4-{[(2S,3R)-2-amino-3- hydroxybutanoyl]amino}- phenyl)ethynyl]-N- [(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]benzamide 440.5 618

4-[(4-{[(2S)-2-amino-4- cyanobutanoyl]amino}- phenyl)ethynyl]-N- [(1S)-1-(aminomethyl)- 2-(hydroxyamino)-2- oxoethyl]benzamide 449.5 619

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-[(4-{[(2S)-2,3- diaminopropanoyl]amino}- phenyl)ethynyl]- benzamide 425.5 620

(2S)-N-(4-{[4-({[(1S)-1- (aminomethyl)-2- (hydroxyamino)-2- oxoethyl]amino}carbonyl)- phenyl]ethynyl}- phenyl)pyrrolidine-2- carboxamide 436.5 621

(2S)-N-(4-{[4-({[(1S)-1- (aminomethyl)-2- (hydroxyamino)-2- oxoethyl]amino}carbonyl)- phenyl]ethynyl}- phenyl)piperidine-2- carboxamide 450.5 622

N-(4-{[4-({[(1S)-1-(amino- methyl)-2-(hydroxyamino)- 2-oxoethyl]amino}carbonyl)- phenyl]ethynyl}- phenyl)piperidine-3-carboxamide 450.5 623

4-[(4-{[(2S)-2-amino-3-(1H-imidaol-4- yl)propanoyl]amino}phenyl)ethynyl]-N-[(1S)- 1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 476.5 624

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- methylphenyl)ethynyl]benzamide 338.4 625

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(2- fluorophenyl)ethynyl]benzamide 342.3 626

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(3- fluorophenyl)ethynyl]benzamide 342.3 627

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- fluorophenyl)ethynyl]benzamide 342.3 628

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- chlorophenyl)ethynyl]benzamide 358.8 629

4-[(4-{[(2S)-2-amino-4- methylpentanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 467.5 630

4-[(4-{[(2S)-2-amino-4- cyanobutanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 464.5 631

4-[(4-{[(2S)-2,3- diaminopropanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 440.5 632

N-[4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)- carbonyl]phenyl}ethynyl)phenyl]piperidin-3- carboxamide 465.5 633

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({3- [(morpholin-4- ylacetyl)amino]phenyl}ethynyl)benzamide 481.5 634

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(pyrazin- 2-ylethynyl)benzamide 341.3 635

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[3- (1H-imidazol-1- yl)propyl]amino}acetyl)amino]phenyl}ethynyl)- benzamide 519.6 636

N-((1S)-2-(hydroxyamino)-1-{[({[3-(1H- imidazol-1- yl)propyl]amino}acetyl)amino]methyl}-2- oxoethyl)-4-(phenylethynyl)benzamide 489.5 637

4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)- carbonyl]phenyl}ethynyl)benzoic acid 383.4 638

N-(2-{[4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)- carbonyl]phenyl}ethynyl)phenyl]amino}-2- oxoethyl)-1,3-benzodioxole-4-carboxamide 559.5 639

4-({4-[((2R)-2-{[(2R)-2,5- diaminopentanoyl]amino}-4- phenylbutanoyl)amino]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 629.7 640

4-[(4-{[(2R)-2-amino-4- phenylbutanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 515.6 641

4-[(4-{[(2S)-2-amino-3- phenylpropanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 501.6 642

4-{[4-({[(2- aminoethyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1Sm2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 454.5 643

N-{(1S)-2-(hydroxyamino)-1-[({[methyl(1- methylpiperidin-4- yl)amino]acetyl}amino)methyl]-2-oxoethyl}-4- (phenylethynyl)benzamide 492.6 644

4-[(4- {[(cyclobutylamino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 465.5 645

4-[(4- {[(cyclopentylamino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 479.5 646

4-[(4- {[(cyclohexylamino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 493.6 647

4-[(4- {[(cycloheptylamino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 507.6 648

4-[(4- {[(cyclooctylamino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 521.6 649

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(propylamino)acetyl]amino}phenyl)ethynyl] benzamide 453.5 650

4-[(4- {[(hexylamino)acetyl]amino}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 495.6 651

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[(1- methylethyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 453.5 652

4-{[4-({[(1,1- dimethylethyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 467.5 653

4-{[4- ({[ethyl(methyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 453.5 654

4-[(4- {[(diethylamino)acetyl]amino}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 467.5 655

4-{[4-({[(1,1- dimethylethyl)(methyl)amino]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 481.6 656

4-{[4- ({[cyclohexyl(methyl)amino]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 507.6 657

4-{[4-({[bis(1- methylethyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 495.6 658

4-{[4- ({[(cyclohexylmethyl)amino]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 507.6 659

4-{[4-({[(2,3- dimethylcyclohexyl)amino]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 521.6 660

4-{[4-({[(1R,2R,4S)-bicyclo[2.2.1]hept-2- ylamino]acetyl}amino)phenyl]ethynyl}-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 505.6 661

4-[(4-{[({[(1S,2R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2- yl]methyl}amino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 547.7 662

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[4- (trifluoromethyl)piperidin-1- yl]acetyl}amino)phenyl]ethynyl}benzamide 547.5 663

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 504.5 664

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2- chlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 521.0 665

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2- methylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 500.6 666

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[2- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]benzamide 516.6 667

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[2- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 554.5 668

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[({2- [(trifluoromethyl)oxy]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 570.5 669

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 504.5 670

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3- chlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 521.0 671

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3- methylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 500.6 672

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[3- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]benzamide 516.6 673

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[3- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 554.5 674

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[({3- [(trifluoromethyl)oxy]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 570.5 675

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(4- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 504.5 676

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(4- chlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 521.0 677

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(4- methylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 500.6 678

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[4- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl)benzamide 516.6 679

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[4- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 554.5 680

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[4-(1,1- dimethylethyl)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]benzamide 542.6 681

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(1R)-1- phenylethyl]amino}acetyl)amino]phenyl}- ethynyl)benzamide 500.6 682

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(1S)-1- phenylethyl]amino}acetyl)amino]phenyl}- ethynyl)benzamide 500.6 683

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4- ({[(cyclohexylmethyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 492.6 684

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(cyclobutylamino)acetyl]amino}phenyl)- ethynyl]benzamide 450.5 685

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(cyclopentylamino)acetyl]amino}phenyl)- ethynyl]benzamide 464.5 686

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(cyclohexylamino)acetyl]amino}phenyl)- ethynyl]benzamide 478.6 687

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(cycloheptylamino)acetyl]amino}phenyl)- ethynyl]benzamide 492.6 688

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(cyclooctylamino)acetyl]amino}phenyl)- ethynyl]benzamide 506.6 689

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(ethylamino)acetyl]amino}phenyl)ethynyl]- benzamide 424.5 690

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(propylamino)acetyl]amino}phenyl)ethynyl] benzamide 438.5 691

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(butylamino)acetyl]amino}phenyl)ethynyl]- benzamide 452.5 692

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(hexylamino)acetyl]amino}phenyl)ethynyl]- benzamide 480.6 693

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1- methylethyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 438.5 694

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1,1- dimethylethyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 452.5 695

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4- ({[ethyl(methyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 438.5 696

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(diethylamino)acetyl]amino}phenyl)ethynyl] benzamide 452.5 697

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1,1- dimethylethyl)(methyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 466.6 698

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4- ({[cyclohexyl(methyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 492.6 699

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[2-(2- fluorophenyl)ethyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 518.6 700

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[2-(3- fluorophenyl)ethyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 518.6 701

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[2-(4- fluorophenyl)ethyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 518.6 702

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- ocoethyl]-4-({4-[({[(1S,2R)-2- phenylcyclopropyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 512.6 703

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2,4- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 522.5 704

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2,4- dichlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 555.4 705

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[4-fluoro-2- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 572.5 706

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2,5- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 522.5 707

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3,4- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 522.5 708

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3,4- dichlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 555.4 709

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3,4- dimethylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 514.6 710

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3,5- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 522.5 711

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3,5- dichlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 555.4 712

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[3,5- bis(trifluoromethyl)phenyl]methyl}amino)- acetyl]amino}phenyl)ethynyl]benzamide 622.5 713

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(4- nitrophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 531.5 714

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(pyridin-2- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 473.5 715

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(pyridin-3- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 473.5 716

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- fluorophenyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 490.5 717

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(3- fluorophenyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 490.5 718

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(4- fluorophenyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 490.5 719

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(pyridin-4- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 473.5 720

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2,2,2- trifluoroethyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 478.4 721

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(pyridin-2- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 488.5 722

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(pyridin-3- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 488.5 723

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(pyridin-4- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 488.5 724

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[(4- phenylpiperazin-1- yl)acetyl]amino}ethynyl]benzamide 556.6 725

4-{[4-({[4-(4-fluorophenyl)piperazin-1- yl]acetyl}amino)phenyl]ethynyl}-N-{(1S,2R)- 2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 574.6 726

4-{[4-({[(1-acetylpiperidin-4- yl)(cyclopropyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 576.7 727

4-[(4- {[(butylamino)acetyl]amino}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 467.5 728

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(1R)-1- phenylethyl]amino}acetyl)amino]phenyl}- ethynyl)benzamide 515.6 729

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(1S)-1- phenylethyl]amino}acetyl)amino]phenyl}- ethynyl)benzamide 515.6 730

4-{[4- ({[cyclopropyl(methyl)amino]acetyl}amino)- phenyl]ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 465.5 731

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[methyl(phenylmethyl)amino]acetyl}amino) phenyl]ethynyl}benzamide 515.6 732

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4- ({[cyclopropyl(methyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 450.5 733

4-[(4-{[(2S)-2- aminopropanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 425.5 734

4-[(4-{[(2R)-2- aminopropanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 425.5 735

4-[(4-{[(2S)-2-amino-3- methylbutanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 453.5 736

4-[(4-{[(2S,3R)-2-amino-3- hydroxybutanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 455.5 737

(2S)-N-[4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)- carbonyl]phenyl}ethynyl)phenyl]pyrrolidine-2- carboxamide 451.5 738

4-[(4-{[(2S)-2-amino-3-(1H-imidazol-4- yl)propanoyl]amino}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 491.5 739

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(methyloxy)acetyl]amino}phenyl)ethynyl]- benzamide 426.4 740

4-[(4-{[(2S)-2-amino-3- methylbutanoyl]amino}phenyl)ethynyl]-N- [(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 438.5 741

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(3- phenylpropyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 514.6 742

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(thien-2- ylethynyl)benzamide 345.4 743

4-({4-[((2S)-2-{[(2S)-2,5- diaminopentanoyl]amino}-3- phenylpropanoyl)amino]phenyl}ethynyl)-N- {(1R,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 615.7 744

3,4-dihydroxy-N-[(2S)-3-(hydroxyamino)-3- oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)- propyl]benzamide 460.5 745

1,1-dimethylethyl 3-[(2-{[(2S)-3- (hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- amino}-2-oxoethyl)amino]propylcarbamate 538.6 746

N-[(1S)-2-(hydroxyamino)-1-({[(4- methylpiperazin-1-yl)acetyl]amino}methyl)-2- oxoethyl]-4-(phenylethynyl)benzamide 464.5 747

4-{[4-({2-[(2-aminoethyl)amino]-2- oxoethyl}oxy)phenyl]ethynyl}-N-{(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 455.5 748

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[3- (aminomethyl)phenyl]ethynyl}benzamide 353.4 749

1,1-dimethylethyl (2S)-3-(hydroxyamino)-2- [({4-[(4-{[2-(hydroxyamino)-2- oxoethyl]oxy}phenyl)ethynyl]phenyl}carbonyl)- amino]-3-oxopropylcarbamate 513.5 750

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[2-(hydroxyamino)-2- oxoethyl]oxy}phenyl)ethynyl]benzamide 413.4 751

3,4-dihydroxy-N-(2-{[4-({4-[({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]amino}-2- oxoethyl)benzamide 547.5 752

4-({4-[({[(2S)-2,5- diaminopentanoyl]amino}acetyl)amino]phenyl}- ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 525.6 753

4-[(4-{[(2- aminoethyl)amino]carbonyl}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 425.5 754

N-[(1S)-2-[({[(3- aminopropyl)amino]acetyl}amino)methyl]-2- (hydroxyamino)-2-oxoethyl]-4- (phenyethynyl)benzamide 438.5 755

3-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)benzoic acid 383.4 756

4-{[4-({[(3- aminopropyl)amino]acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- (hydroxyamino)carbonyl]propyl}benzamide 468.5 757

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(pyrazin-2-ylethynyl)benzamide 326.3 758

4-({3-[(4- aminobutanoyl)amino]phenyl}ethynyl)-N- [(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 424.5 759

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2S)-2,5- diaminopentanoyl]amino}phenyl)ethynyl]- benzamide 453.5 760

4-({2-[(aminoacetyl)amino]phenyl}ethynyl)-N- [(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 396.4 761

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[2-(ethylamino)-2- oxoethyl]phenyl}ethynyl)benzamide 409.5 762

4-({4-[(aminoacetyl)amino]-3- methylphenyl}ethynyl)-N-[(1S)-1- (aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 410.4 763

4-({4-[(aminoacetyl)amino]phenyl}ethynyl)-N- [(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-3-fluorobenzamide 414.4 764

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4- ({[(cyanomethyl)amino]acetyl}amino)phenyl] ethynyl}benzamide 435.5 765

[4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]acetic acid 397.4 766

4-amino-2-({[4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]carbonyl}amino)-4- oxobutanoic acid 497.5 767

4-amino-2-[({[4-({4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]oxy}acetyl)amino]- 4-oxobutanoic acid 527.5 768

N-((1S)-2-(hydroxyamino)-1-{[(morpholin-4- ylacetyl)amino]methyl}-2-oxoethyl)-4- (phenylethynyl)benzamide 451.5 769

N-[(1S)-1-[({[(2,3- dihydroxypropyl)thio]acetyl}amino)methyl]-2- (hydroxyamino)-2-oxoethyl]-4- (phenylethynyl)benzamide 472.5 770

methyl (2S)-3-amino-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)pro- panoate 323.4 771

N-{(1S)-2-(hydroxyamino)-2-oxo-1-[({[(2- phenylethyl)amino]acetyl}amino)methyl]ethyl}- 4-(phenylethynyl)benzamide 485.6 772

4-[(4-{2-[(2-aminoethyl)amino]-2- oxoethyl}phenyl)ethynyl]-N-{(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 439.5 773

4-[(4-{[(6- aminohexyl)amino]carbonyl}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 481.6 774

4-[4-(4- {[(ethylamino)acetyl]amino}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 463.5 775

4-[4-(4- {[(cyclopropylamino)acetyl]amino}phenyl)- buta-1,3-diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 475.5 776

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [(piperidin-1-ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 503.6 777

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(phenylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 511.5 778

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(phenylmethyl)amino]acetyl}amino)phenyl] buta-1,3-diynyl}benzamide 525.6 779

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4′-ethyl-1,1′- biphenyl-4-carboxamide 342.4 780

4-[(4- {[(dimethylamino)acetyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 439.5 781

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [(pyrrolidin-1- ylacetyl)amino]phenyl}ethynyl)benzamide 465.5 782

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(pentylamino)acetyl]amino}phenyl)ethynyl] benzamide 481.6 783

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[(thien-2- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} benzamide 507.6 784

4-{[4-({[(1H-benzimidazol-2- ylmethyl)amino]acetyl}amino)phenyl]ethynyl}- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 541.6 785

4-{[4-({[(1-benzothien-3- ylmethyl)amino]acetyl}amino)phenyl]ethynyl}- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 557.6 786

4-(4-{4-[({[(2- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 543.6 787

4-(4-{4-[({[(3- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 543.6 788

4-(4-{4-[({[(4- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 543.6 789

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[(2- methylphenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 539.6 790

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[(3- methylphenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 539.6 791

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[(4- methylphenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 539.6 792

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(pyridin-2- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 526.6 793

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(pyridin-3- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 526.6 794

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(pyridin-4- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 526.6 795

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[({[2- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)buta-1,3-diynyl]benzamide 555.6 796

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[({[3- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)buta-1,3-diynyl]benzamide 555.6 797

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[({[4- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)buta-1,3-diynyl]benzamide 555.6 798

4-{4-[4-({[(2- fluorophenyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 529.5 799

4-{4-[4-({[(3- fluorophenyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 529.5 800

4-{4-[4-({[(4- fluorophenyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 529.5 801

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(pyridin-2- ylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 512.5 802

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(pyridin-3- ylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 512.5 803

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(pyridin-4- ylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 512.5 804

4-[4-(4- {[(cyclobutylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 489.5 805

4-[4-(4- {[(cyclopentylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 503.6 806

4-[4-(4- {[(cyclohexylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 517.6 807

4-[4-(4- {[(cycloheptylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 531.6 808

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(methylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 449.5 809

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(propylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 477.5 810

4-[4-(4- {[(butylamino)acetyl]amino}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 491.6 811

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- {[(pentylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 505.6 812

4-[4-(4- {[(hexylamino)acetyl]amino}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 519.6 813

4-{4-[4- ({[ethyl(methyl)amino]acetyl}amino)phenyl]- buta-1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 477.5 814

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(1- methylethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 477.5 815

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(2- methylpropyl)amino]acetyl}amino)phenyl]- buta-1,3-diynyl}benzamide 491.6 816

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(2,2,2- trifluoroethyl)amino]acetyl}amino)phenyl]- buta-1,3-diynyl}benzamide 517.5 817

4-{4-[4-({[(2- hydroxyethyl)amino]acetyl}amino)phenyl]- buta- 1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 479.5 818

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[2- (methyloxy)ethyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 493.5 819

4-(4-{4-[({[2- (dimethylamino)ethyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]propyl}benzamide 506.6 820

4-{4-[4-({[(2- cyanoethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 488.5 821

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [(pyrrolidin-1-ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 489.5 822

4-(4-{4-[(azepan-1- ylacetyl)amino]phenyl}buta-1,3-diynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 517.6 823

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4-{[(4- methylpiperazin-1- yl)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 518.6 824

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [(morpholin-4-ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 505.5 825

4-{4-[4- ({[cyclohexyl(methyl)amino]acetyl}amino)- phenyl]buta-1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 531.6 826

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[(1R)-1- phenylethyl]amino}acetyl)amino]phenyl}buta- 1,3-diynyl)benzamide 539.6 827

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[(1S)-1- phenylethyl]amino}acetyl)amino]phenyl}buta- 1,3-diynyl)benzamide 539.6 828

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[4- ({[(2- phenylethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 539.6 829

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [(1H-imidazol-1-ylacetyl)amino]phenyl}buta- 1,3-diynyl)benzamide 486.5 830

4-{4-[4-({[(1R,2R,4S)-bicyclo[2.2.1]hept-2- ylamino]acetyl}amino)phenyl]buta-1,3- diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 529.6 831

4-{4-[4- ({[(cyclohexylmethyl)amino]acetyl}amino)- phenyl]buta-1,3-diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 531.6 832

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4′-ethyl-2-fluoro-1,1′-biphenyl-4- carboxamide 346.4 833

4-({4-[(aminoacetyl)amino]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3- (methyloxy)benzamide 441.5 834

4′-ethyl-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-2- (methyloxy)-1,1′-biphenyl-4-carboxamide 373.4 835

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-3- (methyloxy)-4-(phenylethynyl)benzamide 369.4 836

4-[(4-ethylphenyl)ethynyl]-N-{(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 367.4 837

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- hydroxyphenyl)ethynyl]benzamide 355.4 838

2-[(2-{[(2S)-3-(hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- amino}-2-oxoethyl)thio]propanoic acid 470.5 839

4-amino-2-[(2-{[(2S)-3-(hydroxyamino)-3-oxo- 2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- amino}-2-oxoethyl)amino]-4-oxobutanoic acid 496.5 840

1,1-dimethylethyl 4-amino-2-[(2-{[(2S)-3- (hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- amino}-2-oxoethyl)amino]-4-oxobutanoate 552.6 841

2,6-dihydroxy-N-[(2S)-3-(hydroxyamino)-3- oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)- propyl]-pyridine-4-carboxamide 461.4 842

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- aminophenyl)ethynyl]benzamide 339.4 843

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- ethylphenyl)ethynyl]benzamide 352.4 844

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-ethylphenyl)ethynyl]-3- fluorobenzamide 370.4 845

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(3- aminopropanoyl)amino]phenyl}ethynyl)- benzamide 410.4 846

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(dimethylamino)acetyl]amino}phenyl)- ethynyl]benzamide 424.5 847

4-({4-[(4- aminobutanoyl)amino]phenyl}ethynyl)-N- [(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 424.5 848

N-{(1S)-2-(hydroxyamino)-1-[({[2- (methyloxy)phenyl]methyl}amino)methyl]-2- oxoethyl}-4-(phenylethynyl)benzamide 444.5 849

N-[(1S)-1-[(diprop-2-enylamino)methyl]-2- (hydroxyamino)-2-oxoethyl]-4- (phenylethynyl)benzamide 404.5 850

N-[(1S)-2-(hydroxyamino)-1-({[({[2- (methyloxy)phenyl]methyl}amino)acetyl]- amino}methyl)-2-oxoethyl]-4- (phenylethynyl)benzamide 501.6 851

N-((1S)-2-(hydroxyamino)-1-{[({[2- (methyloxy)phenyl]thio}acetyl)amino]methyl}- 2-oxoethyl)-4-(phenylethynyl)benzamide 504.6 852

(2S,3R)-3-amino-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)- butanoic acid 323.4 853

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(dimethylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]benzamide 448.5 854

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(ethylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 448.5 855

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(cyclopropylamino)acetyl]amino}phenyl)- buta-1,3-diynyl]benzamide 460.5 856

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(piperidin-1- ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 488.6 857

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(phenylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 496.5 858

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4- ({[(phenylmethyl)amino]acetyl}amino)phenyl] buta-1,3-diynyl}benzamide 510.6 859

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-aminophenyl)buta-1,3- diynyl]benzamide 363.4 860

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(pyrazin-2- ylamino)acetyl]amino}phenyl)ethynyl]- benzamide 489.5 861

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-{[(4- phenylpiperidin-1- yl)acetyl]amino}phenyl)ethynyl]benazmide 555.6 862

4-{[4-({[4-(2-fluorophenyl)piperazin-1- yl]acetyl}amino)phenyl]ethynyl}-N-{(1S,2R)- 2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 574.6 863

4-{[4-({[(1S,4R)-bicyclo[2.2.1]hept-2- ylamino]acetyl}amino)phenyl]ethynyl}-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 505.6 864

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(1S,2S,3S,5R)-2,6,6- trimethylbicyclo[3.1.1]hept-3- yl]amino}acetyl)amino]phenyl}ethynyl)- benzamide 547.7 865

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[(tricyclo[3.3.1.1~3,7~]dec-1- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} benzamide 559.7 866

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[(4- methylcyclohexyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 507.6 867

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[(2,2,2- trifluoroethyl)amino]acetyl}amino)phenyl]- ethynyl}benzamide 493.5 868

4-({4-[({[2-(2- fluorophenyl)ethyl]amino}acetyl)amino]phenyl}- ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 533.6 869

4-({4-[({[2-(3- fluorophenyl)ethyl]amino}acetyl)amino]phenyl}- ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 533.6 870

4-({4-[({[2-(4- fluorophenyl)ethyl]amino}acetyl)amino]phenyl}- ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 533.6 871

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(1S,2R)-2- phenylcyclopropyl]amino}acetyl)amino]phenyl}- ethynyl)benzamide 527.6 872

N-{(1R,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[(2- methylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 515.6 873

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[({[2- (trifluoromethyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 569.5 874

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[({2- [(trifluoromethyl)oxy]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 585.5 875

4-({4-[({[(4- chlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 536.0 876

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[({[4- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]benzamide 531.6 877

4-[(4-{[({[4-(1,1- dimethylethyl)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]propyl}benzamide 557.7 878

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[(4- nitrophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 546.5 879

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[({4- [(trifluoromethyl)oxy]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 585.5 880

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[({[4- (methylthio)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]benzamide 547.6 881

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[({4- [(trifluoromethyl)thio]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 601.6 882

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[({[4- (methylsulfonyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 579.6 883

4-({4-[({[(2,5- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 537.5 884

4-({4-[({[(2,6- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 537.5 885

4-({4-[({[(3,4- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 537.5 886

4-({4-[({[(3,4- dichlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 570.4 887

4-({4-[({[(3,4- dimethylphenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 529.6 888

4-({4-[({[(3,5- dichlorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 570.4 889

4-[(4-{[({[3,5- bis(trifluoromethyl)phenyl]methyl}amino)- acetyl]amino}phenyl)ethynyl]-N-{(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 637.5 890

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(2,3,4- trifluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 555.5 891

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(2,4,5- trifluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 555.5 892

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [({[(3,4,5- trifluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 555.5 893

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(pentylamino)acetyl]amino}phenyl)ethynyl] benzamide 466.6 894

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(thien-2- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} benzamide 492.6 895

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(4-phenylpiperidin-1- yl)acetyl]amino}phenyl)ethynyl]benzamide 540.6 896

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(4-phenylpiperazin-1- yl)acetyl]amino}phenyl)ethynyl]benzamide 541.6 897

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[4-(2- fluorophenyl)piperazin-1- yl]acetyl}amino)phenyl]ethynyl}benzamide 559.6 898

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[4-(4- fluorophenyl)piperazin-1- yl]acetyl}amino)phenyl]ethynyl}benzamide 559.6 899

4-{[4-({[1-acetylpiperidin-4- yl)cyclopropyl)amino]acetyl}amino)phenyl]- ethynyl}-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 561.7 900

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2,3- dimethylcyclohexyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 506.6 901

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1R,2R,4S)- bicyclo[2.2.1]hept-2- ylamino]acetyl}amino)phenyl]ethynyl}- benzamide 490.6 902

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[(1S,2R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2- yl]methyl}amino)acetyl]amino}phenyl)ethynyl]- benzamide 532.7 903

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1S,4R)-bicyclo[2.2.1]hept- 2- ylamino]acetyl}amino)phenyl]ethynyl}- benzamide 490.6 904

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(1S,2S,3S,5R)-2,6,6- trimethylbicyclo[3.1.1]hept-3- yl]amino}acetyl)amino]phenyl}ethynyl)- benzamide 532.7 905

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(tricyclo[3.3.1.1~3,7~]dec- 1- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} benzamide 544.7 906

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2,6- difluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 522.5 907

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[4- (methylthio)phenyl]methyl}amino)acetyl]- amino}phenyl)ethynyl]benzamide 532.6 908

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[({[4- (methylsulfonyl)phenyl]methyl}amino)acetyl] amino}phenyl)ethynyl]benzamide 564.6 909

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[({4- [(trifluoromethyl)thio]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 586.6 910

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[({4- [(trifluoromethyl)oxy]phenyl}methyl)amino]- acetyl}amino)phenyl]ethynyl}benzamide 570.5 911

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2,4,5- trifluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 540.5 912

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(2,3,4- trifluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 540.5 913

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(3,4,5- trifluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 540.5 914

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(pyrrolidin-1- ylacetyl)amino]phenyl}buta-1,3- fiynyl)benzamide 474.5 915

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(azepan-1- ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 502.6 916

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(piperazin-1- ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 489.5 917

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[(4-methylpiperazin-1- yl)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 503.6 918

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(morpholin-4- ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 490.5 919

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4- ({[cyclohexyl(methyl)amino]acetyl}amino)- phenyl]buta-1,3-diynyl}benzamide 516.6 920

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(2- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 528.6 921

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(3- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 528.6 922

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(4- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 528.6 923

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(2- methylphenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 524.6 924

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(3- methylphenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 524.6 925

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(4- methylphenyl)methyl]amino}acetyl)amino]- phenyl}buta-1,3-diynyl)benzamide 524.6 926

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(pyridin-2- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 511.6 927

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(pyridin-3- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 511.6 928

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(pyridin-4- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 511.6 929

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[({[2- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)buta-1,3-diynyl]benzamide 540.6 930

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[({[3- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)buta-1,3-diynyl]benzamide 540.6 931

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[({[4- (methyloxy)phenyl]methyl}amino)acetyl]- amino}phenyl)buta-1,3-diynyl]benzamide 540.6 932

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(2- fluorophenyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 514.5 933

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(3- fluorophenyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 514.5 934

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(4- fluorophenyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 514.5 935

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[(pyridin-2- ylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 497.5 936

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[(pyridin-3- ylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 497.5 937

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-{[(pyridin-4- ylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 497.5 938

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(cyclobutylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]benzamide 474.5 939

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(cyclopentylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]benzamide 488.6 940

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(cyclohexylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]benzamide 502.6 941

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(cycloheptylamino)acetyl]amino}phenyl)buta- 1,3-diynyl]benzamide 516.6 942

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(methylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 434.5 943

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(propylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 462.5 944

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(butylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 476.5 945

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(pentylamino)acetyl]amino}phenyl)buta-1,3- diynyl]benzamide 490.6 946

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4- {[(hexylamino)acetyl]amino}phenyl)-buta-1,3- diynyl]benzamide 504.6 947

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4- ({[ethyl(methyl)amino]acetyl}amino)phenyl]- buta-1,3-diynyl}benzamide 462.5 948

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(1- methylethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 462.5 949

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(2- methylpropyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 476.5 950

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(2- hydroxyethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 464.5 951

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[2- (methyloxy)ethyl]amino}acetyl)amino]phenyl}- buta-1,3-diynyl)benzamide 478.5 952

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[2- (dimethylamino)ethyl]amino}acetyl)amino]- phenyl}-buta-1,3-diynyl)benzamide 491.6 953

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(2- cyanoethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 473.5 954

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(thien-2- ylmethyl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 516.6 955

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(1R)-1- phenylethyl]amino}acetyl)amino]phenyl}buta- 1,3-diynyl)benzamide 524.6 956

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[({[(1S)-1- phenylethyl]amino}acetyl)amino]phenyl}buta- 1,3-diynyl)benzamide 524.6 957

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(2- phenylethyl)amino]acetyl}amino)phenyl]buta- 1,3-diynyl}benzamide 524.6 958

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(1H-imidazol-1- ylacetyl)amino]phenyl}buta-1,3- diynyl)benzamide 471.5 959

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(1R,2R,4S)- bicyclo[2.2.1]hept-2- ylamino]acetyl}amino)phenyl]buta-1,3- diynyl}benzamide 514.6 960

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4- ({[(cyclohexylmethyl)amino]acetyl}amino)- phenyl]buta-1,3-diynyl}benzamide 516.6 961

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(6- piperidin-1-ylpyridin-3-yl)ethynyl]benzamide 423.5 962

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[6-(4- methylpiperazin-1-yl)pyridin-3- yl]ethynyl}benzamide 438.5 963

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(6- piperazin-1-ylpyridin-3-yl)ethynyl]benzamide 424.5 964

4-[(6-azepan-1-ylpyridin-3-yl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 437.5 965

4-{[6-(cyclobutylamino)pyridin-3-yl]ethynyl}- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 409.5 966

4-{[6-(cyclohexylamino)pyridin-3-yl]ethynyl}- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 437.5 967

4-{[6-(butylamino)pyridin-3-yl]ethynyl}-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 411.5 968

4-({6-[(2-hydroxyethyl)amino]pyridin-3- yl}ethynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 399.4 969

4-[(6-{[2-(dimethylamino)ethyl]amino}pyridin- 3-yl)ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 426.5 970

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({6- [(phenylmethyl)amino]pyridin-3- yl}ethynyl)benzamide 445.5 971

4-[(6-{[(4-fluorophenyl)methyl]amino}pyridin- 3-yl)ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 463.5 972

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[6- (pyridin-4-ylamino)pyridin-3- yl]ethynyl}benzamide 432.4 973

4-[(6-chloropyridin-3-yl)ethymnyl]-N-{(1S,2R)- 2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 374.8 974

1,1-dimethylethyl (2S)-2-[({4-[(4- ethylphenyl)ethynyl]phenyl}carbonyl)amino]- 3-(hydroxyamino)-3-oxopropylcarbamate 452.5 975

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[4-({[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]amino}carbonyl)phenyl]buta-1,3- diynyl}benzamide 493.5 976

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- (morpholin-4- ylmethyl)phenyl]ethynyl}benzamide 438.5 977

4-[(4-{[(2- aminoethyl)amino]methyl}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 411.5 978

4-({4-[((2S)-2-amino-5- {[amino(imino)methyl]amino}pentanoyl)amino]- phenyl}ethynyl)-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 495.6 979

(2S)-6-amino-2-({[4-({4-[({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]carbonyl}amino)- hexanoic acid 511.5 980

(2S)-6-amino-2-({[4-({4-[({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]acetyl}amino)hexa- noic acid 525.6 981

5-{[(2S)-3-(hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- amino}-5-oxopentanoic acid 438.4 982

N-(2-aminoethyl)-N′-[(2S)-3-(hydroxyamino)- 3-oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- pentanediamine 480.5 983

N-[(1S)-1-[(2,6-dioxopiperidin-1-yl)methyl]-2- (hydroxyamino)-2-oxoethyl]-4- (phenylethynyl)benzamide 420.4 984

N,N′-bis[(2S)-3-(hydroxyamino)-3-oxo-2-({[4- (phenylethynyl)phenyl]carbonyl}amino)propyl]- pentanediamide 743.8 985

N-((1S)-2-(hydroxyamino)-2-oxo-1-{[({[(1S)- 1- phenylethyl]amino}acetyl)amino]methyl}ethyl)- 4-(phenylethynyl)benzamide 485.6 986

N-{(1S)-2-hydroxy-1- [(hydroxyamino)carbonyl]-2-methylpropyl}-4- (phenylethynyl)benzamide 353.4 987

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(6-piperidin-1-ylpyridin-3- yl)ethynyl]benzamide 408.5 988

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(6-morpholin-4-ylpyridin-3- yl)ethynyl]benzamide 410.4 989

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[6-(4-methylpiperazin-1- yl)pyridin-3-yl]ethynyl}benzamide 423.5 990

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(6-piperazin-1-ylpyridin-3- yl)ethynyl]benzamide 409.5 991

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(6-azepan-1-ylpyridin-3- yl)ethynyl]benzamide 422.5 992

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[6-(cyclobutylamino)pyridin-3- yl]ethynyl}benzamide 394.4 993

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[6-(cyclohexylamino)pyridin-3- yl]ethynyl}benzamide 422.5 994

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[6-(butylamino)pyridin-3- yl]ethynyl}benzamide 396.5 995

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(6-{[2- (methyloxy)ethyl]amino}pyridin-3- yl)ethynyl]benzamide 398.4 996

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- (piperidin-1- ylmethyl)phenyl]ethynyl}benzamide 436.5 997

4-[(4-{[(2S)-2-amino-3-(4- aminophenyl)propanoyl]amino}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 516.6 998

4-((2S)-2-amino-3-{[4-({4-[({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}ethynyl)phenyl]amino}-3- oxopropyl)benzoic acid 545.6 999

573.6 1000

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[1- (hydroxymethyl)-2- methylpropyl]amino}acetyl)amino]phenyl}- ethynyl)benzamide 497.6 1001

4-[4-(3-aminophenyl)buta-1,3-diynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 378.4 1002

4-[4-(3-{[(2- aminoethyl)amino]methyl}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 435.5 1003

5-[(4-{[4-({[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]amino}carbonyl)phenyl]ethynyl}- phenyl)amino]-5-oxopentanoic acid 453.5 1004

N-(2-aminoethyl)-3-{4-[4-({[(1S)-1- (aminomethyl)-2-(hydroxyamino)-2- oxoethyl]amino}carbonyl)phenyl]buta-1,3- diynyl}benzamide 434.5 1005

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[3-(aminomethyl)phenyl]buta- 1,3-diynyl}benzamide 377.4 1006

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[3- (trifluoromethyl)phenyl]buta-1,3- diynyl}benzamide 416.4 1007

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-buta-1,3-diynylbenzamide 272.3 1008

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(2-methylphenyl)buta-1,3- diynyl]benzamide 362.4 1009

4-(4-{4-[(3- aminopropanoyl)amino]phenyl}buta-1,3- diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 449.5 1010

4-[4-(3- {[(aminoacetyl)amino]methyl}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 449.5 1011

4-(4-{3-[(aminoacetyl)amino]phenyl}buta-1,3- diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 435.4 1012

4-[4-(4-{[(2S)-2- aminopropanoyl]amino}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 449.5 1013

4-(4-{4-[(aminoacetyl)amino]phenyl}buta-1,3- diynyl)-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 420.4 1014

4-[4-(3- {[(aminoacetyl)amino]methyl}phenyl)buta-1,3- diynyl]-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 434.5 1015

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4-[(3- aminopropanoyl)amino]phenyl}buta-1,3- diynyl)benzamide 434.5 1016

4-(4-{3-[(aminoacetyl)amino]phenyl}buta-1,3- diynyl)-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 420.4 1017

4-[(4-{[(2S)-2-amino-3-(4- hydroxyphenyl)propanoyl]amino}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 517.6 1018

4-(4-{4-[(aminoacetyl)amino]phenyl}buta-1,3- diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 435.4 1019

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(butylamino)methyl]phenyl}ethynyl)- benzamide 409.5 1020

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-(piperidin-1- ylmethyl)phenyl]ethynyl}benzamide 421.5 1021

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- formylphenyl)ethynyl]benzamide 352.4 1022

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [(methylsulfonyl)amino]phenyl}ethynyl)- benzamide 432.5 1023

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(methylsulfonyl)amino]phenyl}ethynyl)- benzamide 417.5 1024

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(phenylsulfonyl)amino]phenyl}ethynyl)- benzamide 479.5 1025

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-{4- [(phenylsulfonyl)amino]phenyl}buta-1,3- diynyl)benzamide 503.5 1026

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-(morpholin-4- ylmethyl)phenyl]ethynyl}benzamide 423.5 1027

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(4-methylpiperazin-1- yl)methyl]phenyl}ethynyl)benzamide 436.5 1028

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2- hydroxyethyl)amino]methyl}phenyl)ethynyl]- benzamide 397.4 1029

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[2- (methyloxy)ethyl]amino}methyl)phenyl]- ethynyl}benzamide 411.5 1030

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(cyclohexylamino)methyl]phenyl}ethynyl)- benzamide 435.5 1031

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(phenylmethyl)amino]methyl}phenyl)- ethynyl]benzamide 443.5 1032

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(6-chloropyridin-3- yl)ethynyl]benzamide 359.8 1033

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[6-(methyloxy)pyridin-3- yl]amino}acetyl)amino]phenyl}buta-1,3- diynyl)benzamide 542.6 1034

4-{4-[4-({[(6-chloropyridin-3- yl)amino]acetyl}amino)phenyl]buta-1,3- diynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 547.0 1035

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- (pyrrolidin-1- ylmethyl)phenyl]ethynyl}benzamide 422.5 1036

4-({4-[(ethylamino)methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 396.5 1037

4-({4- [(dimethylamino)methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 396.5 1038

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[(4- methylpiperazin-1- yl)methyl]phenyl}ethynyl)benzamide 451.5 1039

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[3- (1H-imidazol-1- yl)propyl]amino}methyl)phenyl]ethynyl}- benzamide 476.5 1040

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-thien-2-ylbuta-1,3- diynyl)benzamide 354.4 1041

N,N,N-triethyl-2-{[4-(4-{4-[({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}buta-1,3-diynyl)phenyl]amino}-2- oxoethanaminium 520.6 1042

4-[4-(2-aminophenyl)buta-1,3-diynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 378.4 1043

4-[4-(3-{[(2- aminoethyl)amino]methyl}phenyl)buta-1,3- diynyl]-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 420.5 1044

4-buta-1,3-diynyl-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 287.3 1045

4-[4-(4-{[(2S)-2-amino-4- methylpentanoyl]amino}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 491.6 1046

(2S)-N-[4-(4-{4-[({[(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}buta-1,3-diynyl)phenyl]pyrrolidine- 2-carboxamide 475.5 1047

(2S)-N-[4-(4-{4-[({(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}buta-1,3-diynyl)phenyl]piperidine- 2-carboxamide 489.5 1048

4-[4-(4-{[(2S)-2,3- diaminopropanoyl]amino}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 464.5 1049

4-[4-(4-{[(2S)-2-amino-3-(1H-imidazol-4- yl)propanoyl]amino}phenyl)buta-1,3-diynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 515.5 1050

N-[1-[(hydroxyamino)carbonyl]-2- (propylamino)propyl]-4-[(4- {[(propylamino)acetyl]amino}phenyl)ethynyl] benzamide 494.6 1051

4-[(4- {[(cyclobutylamino)acetyl]amino}phenyl)- ethynyl]-N-{2-(cyclobutylamino)-1- [(hydroxyamino)carbonyl]propyl}benzamide 518.6 1052

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(cyclopropylamino)carbonyl]amino}phenyl)- ethynyl]benzamide 450.5 1053

1-[(1R,2S)-2-[({4-[(4- {[cyclopropylamino)acetyl]amino}phenyl)- ethynyl]phenyl}carbonyl)amino]-3- (hydroxyamino)-1-methyl-3-oxopropyl]triaza- 1,2-dien-2-ium 477.5 1054

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[(4- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 518.6 1055

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[(3- fluorophenyl)methyl]amino}acetyl)amino]- phenyl}ethynyl)benzamide 518.6 1056

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(propylamino)acetyl]amino}phenyl)ethynyl] benzamide 452.5 1057

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[(phenylmethyl)amino]acetyl}amino)phenyl] ethynyl}benzamide 500.6 1058

1-((1R,2S)-3-(hydroxyamino)-1-methyl-3-oxo- 2-{[(4-{[4- ({[(phenylmethyl)amino]acetyl}amino)phenyl] ethynyl}phenyl)carbonyl]amino}propyl)triaza- 1,2-dien-2-ium 527.6 1059

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(cyclobutylamino)acetyl]amino}phenyl)- ethynyl]benzamide 464.5 1060

1-[(1R,2S)-2-[({4-[(4- {[(cyclobutylamino)acetyl]amino}phenyl)- ethynyl]phenyl}carbonyl)amino]-3- (hydroxyamino)-1-methyl-3-oxopropyl]triaza- 1,2-dien-2-ium 491.5 1061

4-[(4-ethylphenyl)ethynyl]-N-{(1S)-1- [(hydroxyamino)carbonyl]-2- methylpropyl}benzamide 365.4 1062

4-(4-{4-[(ethylamino)methyl]phenyl}buta-1,3- diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 420.5 1063

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(3-aminophenyl)buta-1,3- diynyl]benzamide 363.4 1064

4-(4-{3-[(4-aminobutanoyl)amino]phenyl}buta- 1,3-diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 463.5 1065

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(3- hydroxyphenyl)buta-1,3-diynyl]benzamide 379.4 1066

4-(4-{2-[(aminoacetyl)amino]phenyl}buta-1,3- diynyl)-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 435.4 1067

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[2,4-bis(methyloxy)pyrimidin- 5-yl]buta-1,3-diynyl}benzamide 410.4 1068

(2S)-6-amino-2-{[(4-{4-[4-({[(1S)-1- (aminomethyl)-2-(hydroxyamino)-2- oxoethyl]amino}carbonyl)phenyl]buta-1,3- diynyl}phenyl)carbonyl]amino}hexanoic acid 520.6 1069

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(2-aminophenyl)buta-1,3- diynyl]benzamide 363.4 1070

4-[4-(4-{2-[(2-aminoethyl)amino]-2- oxoethyl}phenyl)buta-1,3-diynyl]-N-[(1S)-1- (aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 448.5 1071

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(2-aminopyrimidin-5-yl)buta- 1,3-diynyl]benzamide 365.4 1072

4-(4-{3-[(4-aminobutanoyl)amino]phenyl}buta- 1,3-diynyl)-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 448.5 1073

4-(4-{2-[(aminoacetyl)amino]phenyl}buta-1,3- diynyl)-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 420.4 1074

4-[4-(4-{2-[(2-aminomethyl)amino]-2- oxoethyl}phenyl)buta-1,3-diynyl]-N-{(1S,2R)- 2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 463.5 1075

4-[4-(4-{[(2,3- dihydroxypropyl)amino]methyl}phenyl)buta- 1,3-diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 466.5 1076

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [({[2- (methyloxy)phenyl]methyl}amino)methyl]- phenyl}buta-1,3-diynyl)benzamide 512.6 1077

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [(pyridin-2-ylamino)methyl]phenyl}buta-1,3- diynyl)benzamide 469.5 1078

4-[4-(4-{[(2- aminoethyl)amino]methyl}phenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 435.5 1079

4-[(4-ethylphenyl)ethynyl]-N-[(1R)-1- [(ethylthio)methyl]-2-(hydroxyamino)-2- oxoethyl]benzamide 397.5 1080

4-[(4-{[(2S)-2- aminopropanol]amino}phenyl)ethynyl]-N- [(1R)-1-[(ethylthio)methyl]-2-(hydroxyamino)- 2-oxoethyl]benzamide 455.5 1081

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(3-chlorophenyl)buta-1,3- diynyl]benzamide 382.8 1082

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[3-(methyloxy)phenyl]buta-1,3- diynyl}benzamide 378.4 1083

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{4- [(methylsulfonyl)amino]phenyl}buta-1,3- diynyl)benzamide 456.5 1084

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-(4-{3- [(methylsulfonyl)amino]phenyl}buta-1,3- diynyl)benzamide 456.5 1085

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-(4-pyrazin-2-ylbuta-1,3- diynyl)benzamide 350.3 1086

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(3- nitrophenyl)buta-1,3-diynyl]benzamide 408.4 1087

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(3- {[(methylsulfonyl)amino]methyl}phenyl)- ethynyl]benzamide 446.5 1088

4-[(2-formylphenyl)ethynyl]-N-{(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 367.4 1089

N-{(1R,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(3- {[(methylsulfonyl)amino]methyl}phenyl)- ethynyl]benzamide 446.5 1090

4-({2-[(aminoacetyl)amino]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 411.4 1091

N-{(1S)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{4-[3- (morpholin-4-ylmethyl)phenyl]buta-1,3- diynyl}benzamide 462.5 1092

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(methylamino)methyl]phenyl}ethynyl)- benzamide 367.4 1093

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(ethylamino)methyl]phenyl}ethynyl)- benzamide 381.4 1094

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(propylamino)methyl]phenyl}ethynyl)- benzamide 395.5 1095

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(pentylamino)methyl]phenyl}ethynyl)- benzamide 423.5 1096

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(hexylamino)methyl]phenyl}ethynyl)- benzamide 437.6 1097

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(1- methylethyl)amino]methyl}phenyl)ethynyl]- benzamide 395.5 1098

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2- methylpropyl)amino]methyl}phenyl)ethynyl]- benzamide 409.5 1099

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(1,1- dimethylethyl)amino]methyl}phenyl)ethynyl]- benzamide 409.5 1100

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [dimethylamino)methyl]phenyl}ethynyl)- benzamide 381.4 1101

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[ethyl(methyl)amino]methyl}phenyl)ethynyl] benzamide 395.5 1102

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[2- (dimethylamino)ethyl]amino}methyl)phenyl]- ethynyl}benzamide 424.5 1103

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[4- (dimethylamino)butyl]amino}methyl)phenyl]- ethynyl}benzamide 452.6 1104

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2- cyanoethyl)amino]methyl}phenyl)ethynyl]- benzamide 406.5 1105

4-{[4-({[2- (acetylamino)ethyl]amino}methyl)phenyl]- ethynyl}-N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]benzamide 438.5 1106

4-[(4-{[(2- aminoethyl)amino]methyl}phenyl)ethynyl]-N- [(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 396.5 1107

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(3- hydroxypropyl)amino]methyl}phenyl)ethynyl] benzamide 411.5 1108

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[3- (methyloxy)propyl]amino}methyl)phenyl]- ethynyl}benzamide 425.5 1109

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({methyl[2- (methyloxy)ethyl]amino}methyl)phenyl]- ethynyl}benzamide 425.5 1110

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[3-(2-oxopyrrolidin-1- yl)propyl]amino}methyl)phenyl]ethynyl}- benzamide 478.6 1111

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(3-morpholin-4- ylpropyl)amino]methyl}phenyl)ethynyl]- benzamide 480.6 1112

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(cyclopropylamino)methyl]phenyl}ethynyl)- benzamide 393.5 1113

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(cyclobutylamino)methyl]phenyl}ethynyl)- benzamide 407.5 1114

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(cyclopentylamino)methyl]phenyl}ethynyl)- benzamide 421.5 1115

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(cycloheptylamino)methyl]phenyl}ethynyl)- benzamide 449.6 1116

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(cyclooctylamino)methyl]phenyl}ethynyl)- benzamide 463.6 1117

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-(pyrrolidin-1- ylmethyl)phenyl]ethynyl}benzamide 407.5 1118

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-(azepan-1- ylmethyl)phenyl]ethynyl}benzamide 435.5 1119

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(3R)-3- (dimethylamino)pyrrolidin-1- yl]methyl}phenyl)ethynyl]benzamide 450.6 1120

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(3S)-3- (dimethylamino)pyrrolidin-1- yl]methyl}phenyl)ethynyl]benzamide 450.6 1121

4-[(4-{[(3R)-3-(acetylamino)pyrrolidin-1- yl]methyl}phenyl)ethynyl]-N-[(1S)-1- (aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 464.5 1122

4-[(4-{[(3S)-3-(acetylamino)pyrrolidin-1- yl]methyl}phenyl)ethynyl]-N-[(1S)-1- (aminomethyl)-2-(hydroxyamino)-2- oxoethyl]benzamide 464.5 1123

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-(1,4′-bipiperidin-1′- ylmethyl)phenyl]ethynyl}benzamide 504.6 1124

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[(cyclohexylmethyl)amino]methyl}phenyl)- ethynyl]benzamide 449.6 1125

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4- {[cyclohexyl(methyl)amino]methyl}phenyl)- ethynyl]benzamide 449.6 1126

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1R)-1- phenylethyl]amino}methyl)phenyl]ethynyl}- benzamide 457.5 1127

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1S)-1- phenylethyl]amino}methyl)phenyl]ethynyl}- benzamide 457.5 1128

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(thien-2- ylmethyl)amino]methyl}phenyl)ethynyl]- benzamide 449.5 1129

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(2- phenylethyl)amino]methyl}phenyl)ethynyl]- benzamide 457.5 1130

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(piperidin-3- ylamino)methyl]phenyl}ethynyl)benzamide 436.5 1131

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(piperidin-4- ylamino)methyl]phenyl}ethynyl)benzamide 436.5 1132

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(piperidin-2- ylmethyl)amino]methyl}phenyl)ethynyl]- benzamide 450.6 1133

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(piperidin-3- ylmethyl)amino]methyl}phenyl)ethynyl]- benzamide 450.6 1134

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2S)-pyrrolidin-2- ylmethyl]amino}methyl)phenyl]ethynyl}- benzamide 436.5 1135

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2S)-pyrrolidin-2- ylmethyl]amino}methyl)phenyl]ethynyl}- benzamide 436.5 1136

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(pyrrolidin-3- ylamino)methyl]phenyl}ethynyl)benzamide 422.5 1137

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- fluorophenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 461.5 1138

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(3- fluorophenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 461.5 1139

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(4- fluorophenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 461.5 1140

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(2- methylphenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 457.5 1141

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(3- methylphenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 457.5 1142

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(4- methylphenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 457.5 1143

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[2- (methyloxy)phenyl]methyl}amino)methyl]- phenyl}ethynyl)benzamide 473.5 1144

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[3- (methyloxy)phenyl]methyl}amino)methyl]- phenyl}ethynyl)benzamide 473.5 1145

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[4- (methyloxy)phenyl]methyl}amino)methyl]- phenyl}ethynyl)benzamide 473.5 1146

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4- [(phenylamino)methyl]phenyl}ethynyl)- benzamide 429.5 1147

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(pyridin-3- ylmethyl)amino]methyl}phenyl)ethynyl]- benzamide 444.5 1148

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(4-phenylpiperidin-1- yl)methyl]phenyl}ethynyl)benzamide 497.6 1149

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[(4-phenylpiperazin-1- yl)methyl]phenyl}ethynyl)benzamide 498.6 1150

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(1R,2R,4S)- bicyclo[2.2.1]hept-2- ylamino]methyl}phenyl)ethynyl]benzamide 447.5 1151

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({4-[({[(1S,2R,5S)-6,6- dimethylbicyclo[3.1.1]hept-2- yl]methyl}amino)methyl]phenyl}ethynyl)- benzamide 489.6 1152

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(4-{[(1S,4R)-bicyclo[2.2.1]hept- 2-ylamino]methyl}phenyl)ethynyl]benzamide 447.5 1153

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{[4-({[(1S,2S,3S,5R)-2,6,6- trimethylbicyclo[3.1.1]hept-3- yl]amino}methyl)phenyl]ethynyl}benzamide 489.6 1154

1-((1R,2S)-3-(hydroxyamino)-1-methyl-3-oxo- 2-{[(4-{[4-({[(pyridin-4- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} phenyl)carbonyl]amino}propyl)triaza-1,2-dien- 2-ium 528.6 1155

1-((1R,2S)-2-(hydroxyamino)-1-methyl-3-oxo- 2-{[(4-{[4-({[(pyridin-3- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} phenyl)carbonyl]amino}propyl)triaza-1,2-dien- 2-ium 528.6 1156

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[(pyridin-4- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} benzamide 501.6 1157

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-{[4- ({[(pyridin-3- ylmethyl)amino]acetyl}amino)phenyl]ethynyl} benzamide 501.6 1158

N-[1-[(hydroxyamino)carbonyl]-2- (methylamino)propyl]-4-{[4- ({[(phenylmethyl)amino]acetyl}amino)phenyl] ethynyl}benzamide 514.6 1159

4-[(4- {[(cyclobutylamino)acetyl]amino}phenyl)- ethynyl]-N-[1-[(hydroxyamino)carbonyl]-2- (methylamino)propyl]benzamide 478.6 1160

4-[(4-{[(2S)-2- aminopropanoyl]amino}phenyl)ethynyl]-N- [(1R)-1-{[ethyl(hydroxy)-lambda~4~- sulfanyl]methyl}-2-(hydroxyamino)-2- oxoethyl]benzamide 473.6 1161

4-[(4-ethylphenyl)ethynyl]-N- hydroxybenzamide 266.3 1162

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(2,4-difluorophenyl)buta-1,3- diynyl]benzamide 384.4 1163

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[(2- aminophenyl)ethynyl]benzamide 339.4 1164

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(3- {[(methylsulfonyl)amino]methyl}phenyl)buta- 1,3-diynyl]benzamide 455.5 1165

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(3- {[(methylsulfonyl)amino]methyl}phenyl)buta- 1,3-diynyl]benzamide 455.5 1166

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-({3- [(methylsulfonyl)amino]phenyl}ethynyl)- benzamide 417.5 1167

4-[(4-{[(2S)-2- aminopropanoyl]amino}phenyl)ethynyl]-N- hydroxybenzamide 324.4 1168

4-[(2-{[(2- aminoethyl)amino]methyl}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 411.5 1169

N-{(1R,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4- (phenylethynyl)benzamide 338.4 1170

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-[4-(4- aminophenyl)buta-1,3-diynyl]benzamide 377.4 1171

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(3-hydroxyphenyl)buta-1,3- diynyl]benzamide 364.4 1172

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-{4-[3-(morpholin-4- ylmethyl)phenyl]buta-1,3-diynyl}benzamide 447.5 1173

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4-[({[2- (methyloxy)phenyl]methyl}amino)methyl]- phenyl}ethynyl)benzamide 488.6 1174

4-[(4-{[(2,3- dihydroxypropyl)amino]methyl}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 442.5 1175

4-({2- [(dimethylamino)methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 396.5 1176

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [(methylamino)methyl]phenyl}ethynyl)- benzamide 382.4 1177

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [(propylamino)methyl]phenyl}ethynyl)- benzamide 410.5 1178

4-({4-[(butylamino)methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 424.5 1179

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [(pentylamino)methyl]phenyl}ethynyl)- benzamide 438.5 1180

4-({4-[(hexylamino)methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 452.6 1181

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[(1- methylethyl)amino]methyl}phenyl)ethynyl]- benzamide 410.5 1182

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4-{[(2- methylpropyl)amino]methyl}phenyl)ethynyl]- benzamide 424.5 1183

4-[(4-{[(1,1- dimethylethyl)amino]methyl}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 424.5 1184

4-[(4-{[ethyl(methyl)amino]- methyl}phenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}- benzamide 410.5 1185

4-{[4-({[2-(dimethylamino)- ethyl]amino}methyl)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 439.5 1186

4-{[4-({[4- (dimethylamino)butyl]amino}- methyl)phenyl]ethynyl}- -N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 467.6 1187

4-[(4-{[(2-hydroxyethyl)- amino]methyl}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 412.5 1188

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(3-hydroxy- propyl)amino]methyl}- phenyl)ethynyl]benzamide 426.5 1189

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({methyl[2- (methyloxy)ethyl]amino}- methyl)phenyl]- ethynyl}benzamide 440.5 1190

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[2-(methyl- oxy)ethyl]amino}methyl)- phenyl]ethynyl}benzamide 426.5 1191

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[3-(methyl- oxy)propyl]amino}methyl)phenyl]- ethynyl}benzamide 440.5 1192

4-[(4-{[(2-cyanoethyl)- amino]methyl}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 421.5 1193

4-{[4-({[2- (acetylamino)ethyl]amino}- methyl)phenyl]- ethynyl}-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 453.5 1194

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[3- (2-oxopyrrolidin-1- yl)propyl]amino}methyl)- phenyl]ethynyl}- benzamide 493.6 1195

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(3-morpholin- 4-ylpropyl)amino]methyl}- phenyl)ethynyl]- benzamide 495.6 1196

4-({4-[(cyclopropylamino)methyl]- phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 408.5 1197

4-({4-[(cyclobutylamino)- methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 422.5 1198

4-({4-[(cyclopentylamino)methyl]- phenyl}ethynyl)-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)carbonyl]- propyl}benzamide 436.5 1199

4-({4-[(cyclohexylamino)methyl]- phenyl}ethynyl)-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 450.5 1200

4-({4-[(cycloheptylamino)- methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 464.6 1201

4-({4-[(cyclooctylamino)methyl]- phenyl}ethynyl)-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 478.6 1202

4-{[4-(azepan-1-ylmethyl)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 450.5 1203

4-[(4-{[(3R)-3-(dimethylamino)- pyrrolidin-1-yl]methyl}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 465.6 1204

4-[(4-{[(3S)-2-(dimethylamino)- pyrrolidin-1-yl]methyl}phenyl)- ethynyl]-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 465.6 1205

4-[(4-{[(3R)-3-(acetylamino)- pyrrolidin-1-yl]methyl}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 479.5 1206

4-[(4-{[(3S)-3-(acetylamino)- pyrrolidin-1-yl]methyl}phenyl)- ethynyl]-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 479.5 1207

4-{[4-(1,4′-bipiperidin-1′- ylmethyl)phenyl]ethynyl}-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 519.7 1208

4-[(4-{[(cyclohexylmethyl)- amino]methyl}phenyl)- ethynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 464.6 1209

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-({4-[(4-phenylpiperazin-1- yl)methyl]phenyl}ethynyl)- benzamide 513.6 1210

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(2- phenylethyl)amino]methyl}- phenyl)ethynyl]- benzamide 472.6 1211

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(1R)-1- phenylethyl]amino}methyl)- phenyl]ethynyl}- benzamide 472.6 1212

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(1S)-1- phenylethyl]amino}methyl)- phenyl]ethynyl}- benzamide 472.6 1213

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(thien-2- ylmethyl)amino]methyl}- phenyl)ethynyl]- benzamide 464.6 1214

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(piperidin-3- ylamino)methyl]phenyl}- ethynyl)benzamide 451.5 1215

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(piperidin-4- ylamino)methyl]phenyl}ethynyl)- benzamide 451.5 1216

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(piperidin-2- ylmethyl)amino]methyl}- phenyl)ethynyl]- benzamide 465.6 1217

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-[(4-{[(piperidin-3- ylmethyl)amino]methyl}- phenyl)ethynyl]- benzamide 465.6 1218

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4- ({[(2R)-pyrrolidin-2- ylmethyl]amino}methyl)- phenyl]ethynyl}- benzamide 451.5 1219

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[(2S)-pyrrolidin- 2-ylmethyl]amino}methyl)- phenyl]ethynyl}- benzamide 451.5 1220

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[(pyrrolidin-3- ylamino)methyl]phenyl}- ethynyl)benzamide 437.5 1221

4-{[4-({[(2- fluorophenyl)methyl]amino}- methyl)phenyl]-ethynyl}-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 476.5 1222

4-{[4-({[(3-fluorophenyl)- methyl]amino}methyl)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 476.5 1223

4-{[4-({[(4-fluorophenyl)- methyl]amino}methyl)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 476.5 1224

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[(2- methylphenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 472.6 1225

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[(3- methylphenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 472.6 1226

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-{[4-({[(4- methylphenyl)methyl]amino}methyl)phenyl]- ethynyl}benzamide 472.6 1227

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(phenylmethyl)amino]methyl}phenyl)- ethynyl]benzamide 458.5 1228

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-({4- [(phenylamino)methyl]phenyl}ethynyl)- benzamide 444.5 1229

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}-4-[(4- {[(pyridin-3- ylmethyl)amino]methyl}phenyl)ethynyl]- benzamide 459.5 1230

4-[(4-{[(1R,2R,4S)-bicyclo[2.2.1]hept-2- ylamino]methyl}phenyl)ethynyl]-N-{(1S,2R)- 2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 462.6 1231

(3R)-N-hydroxy-3-({[4- (phenylethynyl)phenyl]carbonyl}amino)- piperidine-3-carboxamide 364.4 1232

4-({[4- (phenylethynyl)phenyl]carbonyl}amino)- piperidine-4-carboxylic acid 349.4 1233

N-{(1S)-2-(hydroxyamino)-2-oxo-1-[(2S)- pyrrolidin-2-ylmethyl]ethyl}-4- (phenylethynyl)benzamide 378.4 1234

(3R)-3-{[(4′-ethyl-1,1′-biphenyl-4- yl)carbonyl]amino}-N-hydroxypiperidine-3- carboxamide 368.4 1235

1,1-dimethylethyl 3-(4-{4-[({(1S,2R)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}amino)carbon- yl]phenyl}buta-1,3-diynyl)phenylcarbamate 478.5 1236

4-[4-(3-amino-4-methylphenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 392.4 1237

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(3-amino-4-methylphenyl)buta- 1,3-diynyl]benzamide 377.4 1238

4-(4-{4-[(aminoacetyl)amino]-3- methylphenyl}buta-1,3-diynyl)-N-[(1S)-1- (aminomethyl)-3-(hydroxyamino)-2- oxoethyl]benzamide 434.5 1239

N-{(1S,2R)-2-amino-1- [(hydroxyamino)carbonyl]propyl}-4-(2- phenylethynyl)benzamide 340.4 1240

N-[(2R)-2-amino-3-(hydroxyamino)-3- oxopropyl]-4′-ethyl-1,1′-biphenyl-4- carboxamide 328.4 1241

N-[(2R)-2-amino-3-(hydroxyamino)-3- oxopropyl]-4-(phenylethynyl)benzamide 324.4 1242

N-[(2R)-2-amino-3-(hydroxyamino)-3- oxopropyl]-4-(4- chlorophenyl)cyclohexanecarboxamide 340.8 1243

N-[(2S)-2-amino-3-(hydroxyamino)-3- oxopropyl]-4-(4- chlorophenyl)cyclohexanecarboxamide 340.8 1244

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-[2-(4-methylphenyl)ethyl]- benzamide 342.4 1245

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-[4-(4-aminophenyl)butyl]- benzamide 371.4 1246

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[methyl(pyridin- 2-ylmethyl)amino]acetyl}amino)- phenyl]ethynyl}benzamide 516.6 1247

4-{[4-({[[(2-fluorophenyl)methyl]- (methyl)amino]acetyl}-amino)- phenyl]ethynyl}-N-{(1S,2R)-2- hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 533.6 1248

4-{[4-({[[(3-fluorophenyl)- methyl](methyl)amino]acetyl}- amino)phenyl]ethynyl}-N- {(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}benzamide 533.6 1249

4-{[4-({[[(4-fluorophenyl)- methyl](methyl)amino]acetyl}- amino)phenyl]ethynyl}-N- {(1S,2R)-2-hydroxy-1-[(hydroxy- amino)carbonyl]propyl}benzamide 533.6 1250

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[[(2-fluorophenyl)- methyl](methyl)amino]acetyl}- amino)phenyl]ethynyl}benzamide 518.6 1251

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[[(3-fluorophenyl)- methyl](methyl)amino]acetyl}- amino)phenyl]ethynyl}benzamide 518.6 1252

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4-({[[(4- fluorophenyl)methyl]- (methyl)amino]acetyl}- amino)phenyl]ethynyl}benzamide 518.6 1253

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({methyl[(2- methylphenyl)methyl]amino}- acetyl)amino]- phenyl}ethynyl)benzamide 514.6 1254

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-({4-[({methyl[(4- methylphenyl)methyl]amino}- acetyl)amino]- phenyl}ethynyl)benzamide 514.6 1255

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2- oxoethyl]-4-{[4- ({[methyl(phenylmethyl)- amino]acetyl}amino) phenyl]ethynyl}benzamide 500.6 1256

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4- ({[methyl(propyl)amino]acetyl}- amino)phenyl] ethynyl}benzamide 467.5 1257

4-{[4-({[butyl(methyl)amino]- acetyl}amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 481.6 1258

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4- ({[methyl(pentyl)amino]- acetyl}amino)phenyl] ethynyl}benzamide 495.6 1259

4-{[4- ({[hexyl(methyl)amino]acetyl}- amino)phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 509.6 1260

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- 4-{[4-({[methyl(1- methylethyl)amino]acetyl}- amino)phenyl]- ethynyl}benzamide 467.5 1261

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-({[methyl(2- methylpropyl)amino]acetyl}- amino)phenyl]ethynyl}- benzamide 481.6 1262

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({methyl[(2- methylphenyl)methyl]amino}- acetyl)amino]phenyl}ethynyl)- benzamide 529.6 1263

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-({4-[({methyl[(4- methylphenyl)methyl]amino}- acetyl)amino]phenyl}ethynyl)- benzamide 529.6 1264

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[methyl(propyl)amino]- acetyl}amino)phenyl] ethynyl}benzamide 452.5 1265

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[butyl(methyl)amino]- acetyl}amino)phenyl]- ethynyl}benzamide 466.6 1266

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[methyl(pentyl)amino]- acetyl}amino)phenyl]ethynyl}- benzamide 480.6 1267

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[hexyl(methyl)amino]- acetyl}amino)phenyl]ethynyl}- benzamide 494.6 1268

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[methyl(1-methylethyl)- amino]acetyl}amino)phenyl]- ethynyl}benzamide 452.5 1269

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[methyl(2-methylpropyl)- amino]acetyl}amino)phenyl]- ethynyl}benzamide 466.6 1270

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[methyl(pyridin-2- ylmethyl)amino]acetyl}amino)- phenyl]ethynyl} benzamide 501.6 1271

4-{[4-({[(3,4-dihydroxyphenyl)- methyl]amino}methyl)-phenyl]- ethynyl}-N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]propyl}- benzamide 490.5 1272

4-({2-[(aminoacetyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 411.4 1273

4-[(4-{[(2S)-2-aminopro- panoyl]amino}phenyl)ethynyl]- N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 425.5 1274

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-(diethylamino)phenyl]- ethynyl}benzamide 395.5 1275

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{4-[4-(ethylamino)phenyl]buta- 1,3-diynyl}benzamide 391.4 1276

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-[(4-{[(2-amino-2-oxoethyl)- amino]methyl}phenyl)ethynyl]- benzamide 410.4 1277

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-({[1-(hydroxymethyl)-2- methylpropyl]amino}methyl)- phenyl]ethynyl}benzamide 439.5 1278

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-({4-[(pyridin-2-ylamino)- methyl]phenyl}ethynyl)benzamide 430.5 1279

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{4-[3-(ethylamino)phenyl]- buta-1,3-diynyl}benzamide 391.4 1280

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[3-(ethylamino)phenyl]- ethynyl}benzamide 367.4 1281

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-(hydroxymethyl)- phenyl]ethynyl}benzamide 354.4 1282

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[3-(diethylamino)phenyl]- ethynyl}benzamide 395.5 1283

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-{[4-(morpholin-4- ylmethyl)phenyl]ethynyl}- benzamide 438.5 1284

4-({4-[(dimethylamino)- methyl]phenyl}ethynyl)-N- {(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}benzamide 396.5 1285

4-[(4-aminophenyl)ethynyl]-N- {(1S,2R)-2-hydroxy-1-[(hy- droxyamino)carbonyl]propyl}- benzamide 354.4 1286

4-[4-(4-aminophenyl)buta-1,3- diynyl]-N-{(1S,2R)-2-hydroxy- 1-[(hydroxyamino)carbonyl]- propyl}benzamide 378.4 1287

1,1-dimethylethyl 4-(4-{4-[({(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}amino)- carbonyl]phenyl}buta-1,3-diynyl)- phenylcarbamate 478.5 1288

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{4-[4-({[1-(hydroxymethyl)-2- methylpropyl]amino}methyl)- phenyl]buta-1,3- diynyl}benzamide 463.5 1289

N-[(1S)-1-(aminomethyl)-2-(hydroxyamino)-2- oxoethyl]-4-[4-(4-hydroxyphenyl)buta-1,3- diynyl]benzamide 364.4 1290

4-[(2,4-difluorophenyl)ethynyl]-N-{(1S,2S)-2- hydroxy-1- [(hydroxyamino)carbonyl]propyl}benzamide 375.3 1291

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{4-[4-(morpholin-4- ylmethyl)phenyl]buta-1,3- diynyl}benzamide 447.5 1292

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{4-[4-(hydroxymethyl)- phenyl]buta-1,3- diynyl}benzamide 378.4 1293

4-({3-[(2-aminoethyl)amino]- phenyl}ethynyl)-N-{(1S,2R)- 2-hydroxy-1-[(hydroxyamino)- carbonyl]propyl}benzamide 397.4 1294

N-[(1S)-1-(aminomethyl)-2- (hydroxyamino)-2-oxoethyl]- 4-{[4-(trifluoromethyl)- phenyl]ethynyl}benzamide 392.3 1295

(2S,3R)-3-hydroxy-2-({[4- (phenylethynyl)phenyl]- carbonyl}amino)- butanoic acid 324.3 1296

N-((1S,2R)-1-{[(2- aminoethyl)amino]carbonyl}- 2-hydroxypropyl)-4-(phenyl- ethynyl)benzamide 366.4 1297

1,1-dimethylethyl (2S)-3- (hydroxyamino)-3-oxo-2- ({[4-(4-phenylbuta-1,3- diynyl)phenyl]carbonyl}- amino)propylcarbamate 448.5 1298

N-{(1S,2R)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-(4-{4-[(3-morpho- lin-4-ylpropyl)amino]phenyl}- buta-1,3-diynyl)benzamide 505.6 1299

N-[(1S,2R)-2-hydroxy-1-({[2- (methylthio)phenyl]amino}- carbonyl)propyl]-4- (phenylethynyl)benzamide 445.6 1300

N-{(1S,2R)-2-hydroxy-1- [(pyridin-2-ylamino)car- bonyl]propyl}-4-(phenyl- ethynyl)benzamide 400.4 1301

N-((1S)-1-(aminomethyl)-2- {[(1,1-dimethylethyl)oxy]- amino}-2-oxoethyl)-4-(4- phenylbuta-1,3-diynyl)- benzamide 404.5 1302

N-{(1S,2S)-2-hydroxy-1- [(hydroxyamino)carbonyl]- propyl}-4-(4-phenylbuta- 1,3-diynyl)benzamide 363.4 1303

(2S,3R)-N,3-dihydroxy-2-({[4- (4-phenylbuta-1,3-diynyl)- phenyl]methyl}amino)- butanamide 349.4 1304

1,1-dimethylethyl (2S)-3- (hydroxyamino)-3-oxo-2- ({[4-(4-phenylbuta-1,3- diynyl)phenyl]methyl}- amino)propylcarbamate 434.5 1305

(2S)-3-amino-N-hydroxy-2- ({[4-(4-phenylbuta-1,3- diynyl)phenyl]methyl}- amino)propanamide 334.4 1306

N-[(1S)-2-(hydroxyamino)-1- (hydroxymethyl)-2-oxoethyl]-4- [(trifluoromethyl)oxy]benzamide 309.2 1307

N-{2-hydroxy-1-[(hydroxyamino)- carbonyl]-2-phenylethyl}-4- [(trifluoromethyl)oxy]benzamide 385.3 

1. A compound according to the formula IA:

or a stereoisomer, pharmaceutically acceptable salt, ester, or prodrug thereof, wherein D is absent or selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; Y is selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted heterocyclyl; and (3) substituted heteroaryl; R₄ is H or substituted or unsubstituted C₁-C₆-alkyl; A is selected from the group consisting of (1) —C(R^(1a), R^(2a))OR^(3a); and (2) —C(R^(1a), R^(2a))N(R^(4a), R^(5a)); wherein R^(1a), R^(2a), R^(3a), R^(4a), and R^(5a) are independently selected from the group consisting of (1) H; and (2) substituted and unsubstituted C₁-C₆-alkyl.
 2. The compound of claim 1, wherein A is —C(R^(1a),R^(2a))OR^(3a).
 3. The compound of claim 2, wherein A is —CH₂OH.
 4. The compound of claim 2, wherein A is —CH(CH₃)OH.
 5. A compound according to the formula IB:

or a stereoisomer, pharmaceutically acceptable salt, ester, or prodrug thereof, wherein D is absent or selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; G is —C≡C—C≡C—; Y is selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; R₄ is H or substituted or unsubstituted C₁-C₆-alkyl; A is —C(R^(1a),R^(2a))N(R^(4a),R^(5a)); wherein R^(1a), R^(2a), R^(4a), and R^(5a) are independently selected from the group consisting of (1) H; and (2) substituted and unsubstituted C₁-C₆-alkyl.
 6. A compound according to Formula VIII:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is selected from the group consisting of (1) H, (2) substituted or unsubstituted C₁-C₆-alkyl, (3) substituted or unsubstituted aryl, (4) substituted or unsubstituted heterocyclyl, and (5) substituted or unsubstituted heteroaryl, or E and R^(3L), together with the atoms to which they are attached form a substituted or unsubstituted heterocyclic ring, having from 5 to 10 ring atoms, wherein 1-4 ring atoms of the heterocyclic ring system are selected from N, O and S; R^(1L), R^(3L) are independently selected from the group consisting of (1) H, (2) substituted or unsubstituted C₁-C₆-alkyl, (3) C₁-C₆-alkyl substituted with aryl, (4) C₁-C₆-alkyl substituted with heterocyclyl, and (5) C₁-C₆-alkyl substituted with heteroaryl, or R^(1L) and R^(3L), together with the atoms to which they are attached form a substituted or unsubstituted heterocyclic ring, having from 5 to 7 ring atoms, wherein 1-2 ring atoms of the heterocyclic ring system are selected from N, O and S.
 7. A compound of claim 5 according to Formula IX:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is selected from the group consisting of (1) H, (2) substituted or unsubstituted C₁-C₆-alkyl, (3) substituted or unsubstituted aryl, (4) substituted or unsubstituted heterocyclyl, and (5) substituted or unsubstituted heteroaryl, or E and R^(3L), together with the atoms to which they are attached form a substituted or unsubstituted heterocyclic ring, having from 5 to 10 ring atoms, wherein 1-4 ring atoms of the heterocyclic ring system are selected from N, O and S; R^(1L), R^(3L) are independently selected from the group consisting of (1) H, (2) substituted or unsubstituted C₁-C₆-alkyl, (3) C₁-C₆-alkyl substituted with aryl, (4) C₁-C₆-alkyl substituted with heterocyclyl, and (5) C₁-C₆-alkyl substituted with heteroaryl, or R^(1L) and R^(3L), together with the atoms to which they are attached form a substituted or unsubstituted heterocyclic ring, having from 5 to 7 ring atoms, wherein 1-2 ring atoms of the heterocyclic ring system are selected from N, O and S.
 8. A compound of claim 5 according to Formula X:

or stereoisomers, pharmaceutically acceptable salts, esters, and prodrugs thereof, wherein E is selected from the group consisting of (1) H, (2) substituted or unsubstituted C₁-C₆-alkyl, (3) substituted or unsubstituted aryl, (4) substituted or unsubstituted heterocyclyl, and (5) substituted or unsubstituted heteroaryl, or E and R^(3L), together with the atoms to which they are attached form a substituted or unsubstituted heterocyclic ring, having from 5 to 10 ring atoms, wherein 1-4 ring atoms of the heterocyclic ring system are selected from N, O and S; R^(1L), R^(3L) are independently selected from the group consisting of (1) H, (2) substituted or unsubstituted C₁-C₆-alkyl, (3) C₁-C₆-alkyl substituted with aryl, (4) C₁-C₆-alkyl substituted with heterocyclyl, and (5) C₁-C₆-alkyl substituted with heteroaryl, or R^(1L) and R^(3L), together with the atoms to which they are attached form a substituted or unsubstituted heterocyclic ring, having from 5 to 7 ring atoms, wherein 1-2 ring atoms of the heterocyclic ring system are selected from N, O and S.
 9. A compound according to the formula IA:

or a stereoisomer, pharmaceutically acceptable salt, ester, or prodrug thereof, wherein D is absent or selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; Y is selected from the group consisting of (1) substituted or unsubstituted aryl; (2) substituted or unsubstituted heterocyclyl; and (3) substituted or unsubstituted heteroaryl; R₄ is H or substituted or unsubstituted C₁-C₆-alkyl; A is —C(R^(1a),R^(2a))N(R^(4a),R^(5a)); wherein R^(1a), R^(2a), R^(4a), and R^(5a) are independently selected from the group consisting of (1) H; and (2) substituted and unsubstituted C₁-C₆-alkyl.
 10. The compound of claim 9, wherein A is —CH₂NH₂.
 11. The compound of claim 9, wherein A is —CH(CH₃)NH₂.
 12. The compound of claim 9, wherein D is absent and Y is a substituted or unsubstituted aryl.
 13. The compound of claim 9, wherein D is a substituted or unsubstituted aryl and Y is a substituted or unsubstituted aryl.
 14. A compound according to the formula IA:

or a stereoisomer, pharmaceutically acceptable salt, ester, or prodrug thereof, wherein D is absent or selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; Y is an unsubstituted aryl; R₄ is H or substituted or unsubstituted C₁-C₆-alkyl; and A is —CH₂OH.
 15. The compound of claim 14, wherein D is absent.
 16. The compound of claim 14, wherein D is a substituted or unsubstituted aryl.
 17. A compound according to the formula IA:

or a stereoisomer, pharmaceutically acceptable salt, ester, or prodrug thereof, wherein D is absent or selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; Y is selected from the group consisting of (1) substituted aryl; and (2) substituted heterocyclyl; and (3) substituted heteroaryl; R₄ is H or substituted or unsubstituted C₁-C₆-alkyl; and A is —CH(CH₃)OH.
 18. The compound of claim 17, wherein D is absent and Y is a substituted aryl.
 19. A compound according to the formula IA:

or a stereoisomer, pharmaceutically acceptable salt, ester, or prodrug thereof, wherein D is selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; Y is selected from the group consisting of (1) substituted or unsubstituted C₃-C₈-cycloalkyl; (2) substituted or unsubstituted aryl; (3) substituted or unsubstituted heterocyclyl; and (4) substituted or unsubstituted heteroaryl; R₄ is H or substituted or unsubstituted C₁-C₆-alkyl; A is selected from the group consisting of (1) —C(R^(1a),R^(2a))OR^(3a); and (2) —C(R^(1a),R^(2a))N(R^(4a),R^(5a)); wherein R^(1a), R^(2a), R^(3a), R^(4a), and R^(5a) are independently selected from the group consisting of (1) H; and (2) substituted and unsubstituted C₁-C₆-alkyl.
 20. A pharmaceutical composition comprising the compound of claim 1 and a pharmaceutically acceptable excipient.
 21. A pharmaceutical composition comprising the compound of claim 5 and a pharmaceutically acceptable excipient.
 22. A pharmaceutical composition comprising the compound of claim 6 and a pharmaceutically acceptable excipient.
 23. A pharmaceutical composition comprising the compound of claim 9 and a pharmaceutically acceptable excipient.
 24. A pharmaceutical composition comprising the compound of claim 14 and a pharmaceutically acceptable excipient.
 25. A pharmaceutical composition comprising the compound of claim 17 and a pharmaceutically acceptable excipient.
 26. A pharmaceutical composition comprising the compound of claim 19 and a pharmaceutically acceptable excipient.
 27. A pharmaceutical composition comprising a compound of claim 1, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 28. A pharmaceutical composition comprising a compound of claim 5, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 29. A pharmaceutical composition comprising a compound of claim 6, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 30. A pharmaceutical composition comprising a compound of claim 9, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 31. A pharmaceutical composition comprising a compound of claim 14, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 32. A pharmaceutical composition comprising a compound of claim 17, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 33. A pharmaceutical composition comprising a compound of claim 19, a second agent, and a pharmaceutically acceptable excipient, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 34. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 1. 35. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 5. 36. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 6. 37. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 9. 38. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 14. 39. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 17. 40. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim
 19. 41. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 1 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 42. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 5 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 43. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 6 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 44. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 9 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 45. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 14 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 46. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 17 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 47. A method of inhibiting LpxC comprising administering to a patient in need thereof, an effective amount of the compound of claim 19 and an effective amount of a second agent, wherein the second agent is an antibacterial agent, an antiendotoxin agent, or an inhaled non-antibacterial agent for the treatment of respiratory tract infection.
 48. The compound of claim 19, wherein D is a substituted or unsubstituted aryl and Y is a substituted or unsubstituted aryl. 